Label: MINOCYCLINE HYDROCHLORIDE tablet, extended release
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NDC Code(s):
68382-531-01,
68382-531-05,
68382-531-06,
68382-531-10, view more68382-531-16, 68382-531-30, 68382-532-01, 68382-532-05, 68382-532-06, 68382-532-10, 68382-532-16, 68382-532-30, 68382-533-01, 68382-533-05, 68382-533-06, 68382-533-10, 68382-533-16, 68382-533-30, 68382-534-01, 68382-534-05, 68382-534-06, 68382-534-10, 68382-534-16, 68382-534-30, 68382-535-01, 68382-535-05, 68382-535-06, 68382-535-10, 68382-535-16, 68382-535-30, 68382-550-01, 68382-550-05, 68382-550-06, 68382-550-10, 68382-550-16, 68382-550-30, 68382-551-01, 68382-551-05, 68382-551-06, 68382-551-10, 68382-551-16, 68382-551-30, 68382-552-01, 68382-552-05, 68382-552-06, 68382-552-10, 68382-552-16, 68382-552-30
- Packager: Zydus Pharmaceuticals (USA) Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated June 5, 2025
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HIGHLIGHTS OF PRESCRIBING INFORMATION
These highlights do not include all the information needed to use MINOCYCLINE HYDROCHLORIDE EXTENDED-RELEASE TABLETS safely and effectively. See full prescribing information for MINOCYCLINE HYDROCHLORIDE EXTENDED-RELEASE TABLETS.
MINOCYCLINE HYDROCHLORIDE extended-release tablets, for oral use
Initial U.S. Approval: 1971
INDICATIONS AND USAGE
Minocycline hydrochloride extended-release tablets are a tetracycline-class drug indicated to treat inflammatory lesions of non-nodular moderate to severe acne vulgaris in patients 12 years of age and older. (1)
Limitations of Use
This formulation of minocycline has not been evaluated in the treatment of infections. To reduce the development of drug-resistant bacteria and to maintain the effectiveness of other antibacterial drugs, use minocycline hydrochloride extended-release tablets only as indicated. (1)
DOSAGE AND ADMINISTRATION
The recommended dosage of minocycline hydrochloride extended-release tablets are approximately 1 mg/kg once daily for 12 weeks. (2)
DOSAGE FORMS AND STRENGTHS
Extended-release tablets: 45 mg, 55 mg, 65 mg, 80 mg, 90 mg, 105 mg, 115 mg and 135 mg (3)
CONTRAINDICATIONS
Known hypersensitivity to any of the tetracyclines. (4)
WARNINGS AND PRECAUTIONS
- Serious Skin/Hypersensitivity Reactions:Minocycline has been associated with anaphylaxis, serious skin reactions, erythema multiforme, and drug rash with eosinophilia and systemic symptoms (DRESS) syndrome. Discontinue immediately if symptoms occur. (5.1)
- Tooth Discoloration and Enamel Hypoplasia:Use during the second and third trimesters of pregnancy, infancy, and childhood up to the age of 8years may cause permanent discoloration of the teeth (yellow-gray-brown). (5.2, 8.1, 8.4)
- Inhibition of Bone Growth:Use during the second and third trimesters of pregnancy, infancy, and childhood up to the age of 8 years may cause reversible inhibition of bone growth. (5.3, 8.1, 8.4)
- Clostridioides difficile-Associated Diarrhea (Antibiotic-Associated Colitis): Discontinue if Clostridioides difficile-associated diarrhea (antibiotic-associated colitis) occurs. (5.4)
- Hepatotoxicity: Discontinue if liver injury is suspected. (5.5)
- Central Nervous System Effects:May cause central nervous system side effects including light-headedness, dizziness, or vertigo. (5.6)
- Idiopathic Intracranial Hypertension: May cause idiopathic intracranial hypertension in adults and adolescents. Discontinue if symptoms occur. (5.7)
- Autoimmune Syndromes: Minocycline has been associated with autoimmune syndromes; discontinue immediately if symptoms occur. (5.8)
- Metabolic Effects: If renal impairment exists, reduce minocycline dosage. (5.9)
ADVERSE REACTIONS
The most commonly observed adverse reactions (incidence >5%) are headache, fatigue, dizziness, and pruritus. (6.1)
To report SUSPECTED ADVERSE REACTIONS, contact Zydus Pharmaceuticals (USA) Inc. at 1-877-993-8779 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
DRUG INTERACTIONS
Patients who are on anticoagulant therapy may require downward adjustment of their anticoagulant dosage. (7.1)
USE IN SPECIFIC POPULATIONS
Lactation: Breastfeeding is not recommended. (8.2)
See 17 for PATIENT COUNSELING INFORMATION and FDA-approved patient labeling.
Revised: 6/2025
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Table of Contents
FULL PRESCRIBING INFORMATION: CONTENTS*
1 INDICATIONS AND USAGE
2 DOSAGE AND ADMINISTRATION
3 DOSAGE FORMS AND STRENGTHS
4 CONTRAINDICATIONS
5 WARNINGS AND PRECAUTIONS
5.1 Serious Skin/Hypersensitivity Reactions
5.2 Tooth Discoloration and Enamel Hypoplasia
5.3 Inhibition of Bone Growth
5.4 Clostridioides difficile-Associated Diarrhea (Antibiotic-Associated Colitis)
5.5 Hepatotoxicity
5.6 Central Nervous System Effects
5.7 Idiopathic Intracranial Hypertension
5.8 Autoimmune Syndromes
5.9 Metabolic Effects
5.10 Photosensitivity
5.11 Tissue Hyperpigmentation
5.12 Development of Drug-Resistant Bacteria
5.13 Superinfection
5.14 Laboratory Monitoring
6 ADVERSE REACTIONS
6.1 Clinical Trials Experience
6.2 Postmarketing Experience
7 DRUG INTERACTIONS
7.1 Anticoagulants
7.2 Penicillin
7.3 Antacids and Iron Preparations
7.4 Drug/Laboratory Test Interactions
8 USE IN SPECIFIC POPULATIONS
8.1 Pregnancy
8.2 Lactation
8.4 Pediatric Use
8.5 Geriatric Use
10 OVERDOSAGE
11 DESCRIPTION
12 CLINICAL PHARMACOLOGY
12.1 Mechanism of Action
12.2 Pharmacodynamics
12.3 Pharmacokinetics
13 NONCLINICAL TOXICOLOGY
13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility
14 CLINICAL STUDIES
16 HOW SUPPLIED/STORAGE AND HANDLING
17 PATIENT COUNSELING INFORMATION
- *
- Sections or subsections omitted from the full prescribing information are not listed.
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1 INDICATIONS AND USAGE
Minocycline hydrochloride extended-release tablets are indicated to treat inflammatory lesions of non-nodular moderate to severe acne vulgaris in patients 12 years of age and older.
Limitations of Use
- Minocycline hydrochloride extended-release tablets did not demonstrate any effect on non-inflammatory acne lesions.
- This formulation of minocycline has not been evaluated in the treatment of infections [see Clinical Studies (14)].
- To reduce the development of drug-resistant bacteria as well as to maintain the effectiveness of other antibacterial drugs, use minocycline hydrochloride extended-release tablets only as indicated [see Warnings and Precautions (5.12)].
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2 DOSAGE AND ADMINISTRATION
The recommended dosage of minocycline hydrochloride extended-release tablets is approximately 1 mg/kg once daily for 12 weeks. Table 1 provides the recommended minocycline hydrochloride extended-release tablets dosage based upon weight ranges.
Patient's
Weight  (kg)
Recommended Dosage
(mg/day)
45 to 49
45
50 to 59
55
60 to 71
65
72 to 84
80
85 to 96
90
97 to 110
105
111 to 125
115
126 to 136
135
Higher dosages have not shown to be of additional benefit in the treatment of inflammatory lesions of acne and may be associated with more acute vestibular adverse reactions.
Swallow tablets whole. Do not chew, crush, or split the extended-release tablets.
Administer minocycline hydrochloride extended-release tablets with or without food [see Clinical Pharmacology (12.3)]. Ingestion of food along with minocycline hydrochloride extended-release tablets may help reduce the risk of esophageal irritation and ulceration.
In patients with renal impairment, decrease the daily dosage by either reducing the recommended individual doses and/or by extending the time intervals between doses [see Warnings and Precautions (5.9)].
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3 DOSAGE FORMS AND STRENGTHS
- 45 mg extended-release tablets are grey colored, modified capsule shaped, biconvex, coated tablets, debossed with "531" on one side and plain on other side.
- 55 mg extended-release tablets are yellow colored, modified capsule shaped, biconvex, coated tablets, debossed with "550" on one side and plain on other side.
- 65 mg extended-release tablets are blue colored, modified capsule shaped, biconvex, coated tablets, debossed with "532" on one side and plain on other side.
- 80 mg extended-release tablets are whitish blue colored, modified capsule shaped, biconvex, coated tablets, debossed with "551" on one side and plain on other side.
- 90 mg extended-release tablets are light yellow colored, modified capsule shaped, biconvex, coated tablets, debossed with "533" on one side and plain on other side.
- 105 mg extended-release tablets are light blue colored, modified capsule shaped, biconvex, coated tablets, debossed with "552" on one side and plain on other side.
- 115 mg extended-release tablets are green colored, modified capsule shaped, biconvex, coated tablets, debossed with "534" on one side and plain on other side.
- 135 mg extended-release tablets are light pink colored, modified capsule shaped, biconvex, coated tablets, debossed with "535" on one side and plain on other side.
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4 CONTRAINDICATIONS
Minocycline hydrochloride extended-release tablet is contraindicated in patients with history of a hypersensitivity reaction to any of the tetracyclines [see Warnings and Precautions (5.1)].
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5 WARNINGS AND PRECAUTIONS
5.1 Serious Skin/Hypersensitivity Reactions
Cases of anaphylaxis, serious skin reactions (e.g., Stevens-Johnson syndrome), erythema multiforme, and drug rash with eosinophilia and systemic symptoms (DRESS) syndrome have been reported postmarketing with minocycline use in patients with acne. DRESS syndrome consists of cutaneous reaction (such as rash or exfoliative dermatitis), eosinophilia, and one or more of the following visceral complications such as: hepatitis, pneumonitis, nephritis, myocarditis, and pericarditis. Fever and lymphadenopathy may be present. In some cases, death has been reported. If this syndrome is recognized, discontinue minocycline immediately.
5.2 Tooth Discoloration and Enamel Hypoplasia
The use of tetracycline-class drugs, including minocycline, during tooth development (second and third trimesters of pregnancy, infancy, and childhood up to the age of 8 years) may cause permanent discoloration of the teeth (yellow-gray -brown). Permanent discoloration of the teeth is more common during long-term use of tetracycline-class drugs but has been observed following repeated short-term courses. Enamel hypoplasia has also been reported. Use of minocycline is not recommended during tooth development.
Advise the patient of the potential risk to the fetus if minocycline is used during the second or third trimester of pregnancy [see Use in Specific Populations (8.1, 8.4)].
5.3 Inhibition of Bone Growth
The use of tetracycline-class drugs, including minocycline, during the second and third trimesters of pregnancy, infancy, and childhood up to the age of 8 years may cause reversible inhibition of bone growth. All tetracyclines, including minocycline, form a stable calcium complex in any bone-forming tissue. A decrease in fibula growth rate has been observed in premature human infants given oral tetracycline in doses of 25 mg/kg every 6 hours. This reaction was shown to be reversible when the drug was discontinued.
Advise the patient of the potential risk to the fetus if minocycline is used during the second or third trimester of pregnancy [see Use in Specific Populations (8.1, 8.4)].
5.4 Clostridioides difficile-Associated Diarrhea (Antibiotic-Associated Colitis)
Clostridioides difficile-associated diarrhea (CDAD) has been reported with nearly all antibacterial agents, including minocycline, and may range in severity from mild diarrhea to fatal colitis.
C. difficile produces toxins A and B which contribute to the development of CDAD. Hypertoxin-producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea following antibiotic use. Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents.
If CDAD is suspected or confirmed, discontinue minocycline.
5.5 Hepatotoxicity
Postmarketing cases of serious liver injury, including irreversible drug-induced hepatitis and fulminant hepatic failure (sometimes fatal), have been reported with minocycline use in the treatment of acne. Discontinue minocycline if liver injury is suspected.
5.6 Central Nervous System Effects
Central nervous system side effects including light-headedness, dizziness, or vertigo have been reported with minocycline therapy. Caution patients who experience these symptoms about driving vehicles or using hazardous machinery while on minocycline. These symptoms may disappear during therapy and usually rapidly disappear when minocycline is discontinued.
5.7 Idiopathic Intracranial Hypertension
Idiopathic intracranial hypertension has been associated with the use of tetracycline-class drugs, including minocycline. Clinical manifestations of idiopathic intracranial hypertension include headache, blurred vision, diplopia, and vision loss; papilledema can be found on fundoscopy. Women of childbearing age who are overweight or have a history of idiopathic intracranial hypertension are at a greater risk for developing idiopathic intracranial hypertension. Avoid concomitant use of isotretinoin and minocycline because isotretinoin, a systemic retinoid, is also known to cause idiopathic intracranial hypertension.
Permanent visual loss may exist, even after the medication is discontinued. If visual disturbance occurs during treatment, prompt ophthalmologic evaluation is warranted. Because intracranial pressure can remain elevated for weeks after drug cessation, monitor patients until they stabilize.
5.8 Autoimmune Syndromes
Tetracyclines have been associated with the development of autoimmune syndromes. The long-term use of minocycline in the treatment of acne has been associated with drug-induced lupus-like syndrome, autoimmune hepatitis, and vasculitis. Sporadic cases of serum sickness have presented shortly after minocycline use. Symptoms may be manifested by fever, rash, arthralgia, and malaise. Evaluate symptomatic patients. If symptoms occur, immediately discontinue use of minocycline.
5.9 Metabolic Effects
The anti-anabolic action of the tetracyclines, including minocycline, may cause an increase in blood urea nitrogen (BUN). In patients with significantly impaired renal function, higher serum levels of tetracycline-class drugs may lead to azotemia, hyperphosphatemia, and acidosis. If renal impairment exists, lower the total doses of minocycline, and if therapy is prolonged, monitor serum levels minocycline.
5.10 Photosensitivity
Photosensitivity manifested by an exaggerated sunburn reaction has been observed in some individuals taking tetracyclines, including minocycline. Advise patients to minimize or avoid exposure to natural or artificial sunlight (e.g., tanning beds or UVA/B treatment) while using minocycline. Instruct patients to use sunscreen products and wear protective apparel (e.g., hat) when exposure to sun cannot be avoided.
5.11 Tissue Hyperpigmentation
Tetracycline-class antibiotics are known to cause hyperpigmentation. Tetracycline therapy may induce hyperpigmentation in many organs, including nails, bone, skin, eyes, thyroid, visceral tissue, oral cavity (e.g., teeth, mucosa, alveolar bone), sclerae and heart valves. Skin and oral pigmentation has been reported to occur independently of time or amount of drug administration, whereas other tissue pigmentation has been reported to occur upon prolonged administration. Skin pigmentation includes diffuse pigmentation as well as over sites of scars or injury.
5.12 Development of Drug-Resistant Bacteria
Bacterial resistance to tetracyclines may develop in patients using minocycline hydrochloride extended-release tablets. Because of the potential for drug-resistant bacteria to develop during the use of minocycline hydrochloride extended-release tablets, it should be used only as indicated.
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6 ADVERSE REACTIONS
The following clinically significant adverse reactions are described elsewhere in the labeling:
- Serious Skin/Hypersensitivity Reactions [see Warnings and Precautions (5.1)]
- Clostridioides difficile-Associated Diarrhea (Antibiotic-Associated Colitis) [see Warnings and Precautions (5.4)]
- Hepatotoxicity [see Warnings and Precautions (5.5)]
- Central Nervous System Effects [see Warnings and Precautions (5.6)]
- Idiopathic Intracranial Hypertension [see Warnings and Precautions (5.7)]
6.1 Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug, and may not reflect the rates observed in practice.
The following table summarizes selected adverse reactions reported in clinical trials at a rate of >1% for minocycline hydrochloride extended-release tablets and higher than placebo.
Adverse Reactions
Minocycline Hydrochloride
Extended-Release Tablets
(1 mg/kg)
N = 674 (%)
PLACEBO
N = 364 (%)
At least one treatment-emergent event
379 (56)
197 (54)
Fatigue
62 (9)
24 (7)
Dizziness
59 (9)
17 (5)
Pruritus
31 (5)
16 (4)
Malaise
26 (4)
9 (3)
Somnolence
13 (2)
3 (1)
Urticaria
10 (2)
1 (0)
Tinnitus
10 (2)
5 (1)
Arthralgia
9 (1)
2 (0)
Vertigo
8 (1)
3 (1)
6.2 Postmarketing Experience
The following adverse reactions have been reported with minocycline hydrochloride use in a variety of indications.
Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.
Skin and hypersensitivity reactions: anaphylaxis, angioedema, DRESS syndrome, erythema multiforme, Stevens-Johnson syndrome, acute febrile neutrophilic dermatosis (Sweet's syndrome), fixed drug eruptions, balanitis, anaphylactoid purpura, photosensitivity, pigmentation of skin and mucous membranes.
Autoimmune conditions: polyarthralgia, pericarditis, exacerbation of systemic lupus, pulmonary infiltrates with eosinophilia, lupus-like syndrome.
Central nervous system: idiopathic intracranial hypertension, bulging fontanels in infants, decreased hearing.
Endocrine: brown-black microscopic thyroid discoloration, abnormal thyroid function.
Oncology: thyroid cancer.
Oral: glossitis, dysphagia, tooth discoloration.
Gastrointestinal: enterocolitis, pancreatitis, hepatitis, liver failure.
Renal: acute renal failure.
Hematology: hemolytic anemia, thrombocytopenia, eosinophilia.
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7 DRUG INTERACTIONS
7.1 Anticoagulants
Because tetracyclines have been shown to depress plasma prothrombin activity, patients who are on anticoagulant therapy may require downward adjustment of their anticoagulant dosage.
7.2 Penicillin
Because bacteriostatic drugs may interfere with the bactericidal action of penicillin, avoid giving minocycline hydrochloride in conjunction with penicillin.
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8 USE IN SPECIFIC POPULATIONS
8.1 Pregnancy
Tetracycline class drugs, including minocycline may cause permanent discoloration of deciduous teeth and reversible inhibition of bone growth when administered during the second and third trimesters of pregnancy [see Warnings and Precautions (5.2, 5.3) and Use in Specific Populations (8.4)]. A few postmarketing cases of limb reductions have been reported over decades of use; however, the association is unclear. The limited data from postmarketing reports are not sufficient to inform a drug-associated risk for birth defects or miscarriage.
In animal reproduction studies conducted in pregnant rats and rabbits, fetuses with bent limb bones were observed following oral administration of minocycline during organogenesis at systemic exposures 3 and 2 times, respectively, the exposure associated with the maximum recommended human dose (MRHD) (see Data).
If a patient becomes pregnant while taking this drug, advise the patient of the risk to the fetus and to discontinue treatment.
The background risk of major birth defects and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively.
Data
Human Data
The use of tetracycline class drugs, including minocycline, during tooth development (second and third trimesters of pregnancy, infancy, and childhood up to the age of 8 years) may cause permanent discoloration of deciduous teeth (yellow-gray-brown). Permanent discoloration of the teeth is more common during long-term use of the drug but has been observed following repeated short-term courses [see Warnings and Precautions (5.2)].
Animal Data
Results of animal studies indicate that tetracyclines cross the placenta, are found in fetal tissues, and can cause delayed skeletal development in the developing fetus. Evidence of embryotoxicity has been noted in animals treated early in pregnancy [see Warnings and Precautions (5.3)].
Minocycline induced skeletal malformations (bent limb bones) in fetuses when administered to pregnant rats and rabbits during the period of organogenesis at doses of 30 mg/kg/day and 100Â mg/kg/day, respectively (3 times the MRHD and 2 times the MRHD on an AUC comparison basis, respectively). Reduced mean fetal body weight was observed in studies in which minocycline was administered to pregnant rats at an oral dose of 10 mg/kg/day (approximately equal to the MRHD on an AUC comparison basis).
Minocycline was assessed for effects on peri- and post-natal development of rats in a study that involved oral administration to pregnant rats during the period of organogenesis through lactation at dosages of 5 mg/kg/day, 10 mg/kg/day, or 50 mg/kg/day. In this study, body weight gain was significantly reduced in pregnant females that received 50 mg/kg/day (2.5 times the MRHD on an AUC comparison basis). No effects of treatment on the duration of the gestation period or the number of live pups born per litter were observed. Gross external anomalies observed in offspring of animals that received minocycline included reduced body size, improperly rotated forelimbs, and reduced size of extremities. No effects were observed on the physical development, behavior, learning ability, or reproduction of the offspring of animals that received minocycline.
8.2 Lactation
Tetracycline-class antibiotics, including minocycline, are present in breast milk following oral administration. There are no data on the effects of minocycline on milk production. Because of the potential for serious adverse reactions, including tooth discoloration and inhibition of bone growth, advise patients that breastfeeding is not recommended during minocycline therapy and for 4 days after the final dose [see Warnings and Precautions (5.2, 5.3)].
8.4 Pediatric Use
The safety and effectiveness of minocycline hydrochloride have been established in pediatric patients 12 years of age and older for the treatment of inflammatory lesions of non-nodular moderate to severe acne vulgaris [see Clinical Studies (14)]. Tooth discoloration and inhibition of bone growth have been observed in pediatric patients [see Warnings and Precaution (5.2, 5.3)]. Use of tetracycline-class antibiotics below the age of 8 is not recommended due to the potential for tooth discoloration [see Warnings and Precautions (5.2)].
Safety and effectiveness of minocycline have not been established in pediatric patients younger than 12 years of age.
8.5 Geriatric Use
Clinical studies of minocycline hydrochloride extended-release tablets did not include sufficient numbers of subjects aged 65 and over to determine whether they respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and concomitant disease or other drug therapy.
- 10 OVERDOSAGE
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11 DESCRIPTION
Minocycline hydrochloride, a semi synthetic derivative of tetracycline, is [4S-(4α,4aα,5aα,12aα)]-4,7-Bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10, 12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide mono hydrochloride. The structural formula is represented below:
                                    C23H27N3O7•HCl            M. W. 493.95
Each minocycline hydrochloride extended-release tablet, USP intended for oral administration contains minocycline hydrochloride equivalent to 45 mg, 55 mg, 65 mg, 80 mg, 90 mg, 105 mg, 115 mg or 135 mg of minocycline. In addition, each tablet contains the following inactive ingredients: colloidal silicon dioxide, hypromellose, lactose monohydrate, magnesium stearate, polyethylene glycol (55 mg, 65 mg, 80 mg, 90 mg, 105 mg, 115 mg and 135 mg only), titanium dioxide and triacetin.
Additionally, the 45 mg tablets contain ferric oxide black and ferric oxide yellow; the 55 mg tablets contain ferric oxide red and ferric oxide yellow; the 65 mg tablets contain FD & C blue #2 aluminum lake; the 80 mg tablets contain FD & C blue #2 aluminum lake and FD & C red #40 aluminum lake; the 90 mg tablets contain D & C yellow #10 aluminum lake, ferric oxide red and ferric oxide yellow; the 105 mg tablets contain FD & C blue #2 aluminum lake and FD & C red #40 aluminum lake; the 115 mg tablets contain FD & C blue #2 aluminum lake and ferric oxide yellow; the 135 mg tablets contain D & C red #27 aluminum lake, D & C yellow #10 aluminum lake and FD & C blue #2 aluminum lake.
USP dissolution test-8 used.
USP organic impurities procedure pending.
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12 CLINICAL PHARMACOLOGY
12.1 Mechanism of Action
The mechanism of action of minocycline hydrochloride extended-release tablets for the treatment of acne is unknown.
12.2 Pharmacodynamics
The pharmacodynamics of minocycline hydrochloride extended-release tablets for the treatment of acne are unknown.
12.3 Pharmacokinetics
Minocycline hydrochloride extended-release tablets are not bioequivalent to non-modified release minocycline products. Based on pharmacokinetic studies in healthy adults, minocycline hydrochloride extended-release tablets produce a delayed Tmax at 3.5 hours to 4 hours as compared to a non-modified release reference minocycline product (Tmax at 2.25 hours to 3 hours). At steady-state (Day 6), the mean AUC(0 to 24) and Cmax were 33.32 mcg×hr/mL and 2.63 mcg/mL for minocycline hydrochloride extended-release tablets and 46.35 mcg×hr/mL and 2.92 mcg/mL for minocycline hydrochloride capsules, respectively. These parameters are based on dose adjusted to 135 mg/day for both products.
A single-dose, four-way crossover study demonstrated that minocycline hydrochloride extended-release tablets used in the study (45 mg, 90 mg, 135 mg) exhibited dose-proportional pharmacokinetics. In another single-dose, five-way crossover pharmacokinetic study, minocycline hydrochloride extended-release tablets 55 mg, 80 mg, and 105 mg were shown to be dose-proportional to minocycline hydrochloride extended-release tablets 90 mg and 135 mg.
When minocycline hydrochloride extended-release tablets were administered concomitantly with a meal that included dairy products, the extent and timing of absorption of minocycline did not differ from that of administration under fasting conditions.
Minocycline is lipid soluble and distributes into the skin and sebum.
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13 NONCLINICAL TOXICOLOGY
13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility
In a carcinogenicity study in which minocycline hydrochloride was orally administered to male and female rats once daily for up to 104 weeks at dosages up to 200 mg/kg/day, minocycline hydrochloride was associated in both sexes with follicular cell tumors of the thyroid gland, including increased incidences of adenomas, carcinomas and the combined incidence of adenomas and carcinomas in males, and adenomas and the combined incidence of adenomas and carcinomas in females. In a carcinogenicity study in which minocycline hydrochloride was orally administered to male and female mice once daily for up to 104 weeks at dosages up to 150 mg/kg/day, exposure to minocycline hydrochloride did not result in a significantly increased incidence of neoplasms in either males or females.
Minocycline was not mutagenic in vitro in a bacterial reverse mutation assay (Ames test) or CHO/HGPRT mammalian cell assay in the presence or absence of metabolic activation. Minocycline was not clastogenic in vitro using human peripheral blood lymphocytes or in vivo in a mouse micronucleus test.
Male and female reproductive performance in rats was unaffected by oral doses of minocycline of up to 300 mg/kg/day (40 times the MRHD on an AUC comparison basis). However, oral administration of 100 mg/kg/day or 300 mg/kg/day of minocycline to male rats (15 to 40 times the MRHD on an AUC comparison basis) adversely affected spermatogenesis. Effects observed at 300 mg/kg/day included a reduced number of sperm cells per gram of epididymis, an apparent reduction in the percentage of sperm that were motile, and (at 100 mg/kg/day and 300 mg/kg/day) increased numbers of morphologically abnormal sperm cells. Morphological abnormalities observed in sperm samples included absent heads, misshapen heads, and abnormal flagella.
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14 CLINICAL STUDIES
The safety and efficacy of minocycline hydrochloride extended-release tablets in the treatment of inflammatory lesions of non-nodular moderate to severe acne vulgaris was assessed in two 12-week, multi-center, randomized, double-blind, placebo-controlled trials in adult and pediatric subjects 12Â years of age and older (Trial 1 and Trial 2). A total of 924 subjects with non-nodular moderate to severe acne vulgaris received minocycline or placebo for a total of 12 weeks. The mean age of subjects was 20Â years and subjects were from the following racial groups: White (73%), Hispanic (13%), Black (11%), Asian/Pacific Islander (2%), and Other (2%).
The two primary efficacy endpoints were:
1) Mean percent change in inflammatory lesion counts from Baseline to 12 weeks.
2) Percentage of subjects with an Evaluator's Global Severity Assessment (EGSA) of clear or almost clear at 12 weeks.
Efficacy results are presented in Table 4.
Trial 1
Trial 2
Minocycline Hydrochloride
Extended-Release Tablets
(1 mg/kg)
N = 300
Placebo
N = 151
Minocycline Hydrochloride
Extended-Release Tablets
(1 mg/kg)
N = 315
Placebo
N = 158
Mean Percent Improvement in Inflammatory Lesions
43.1%
31.7%
45.8%
30.8%
No. (%) of Subjects
Clear or Almost
Clear on the EGSA*
52
(17.3%)
12
(7.9%)
50
(15.9%)
15
(9.5%)
Minocycline hydrochloride extended-release tablets did not demonstrate any effect on non-inflammatory lesions (benefit or worsening).
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16 HOW SUPPLIED/STORAGE AND HANDLING
Minocycline Hydrochloride Extended-release Tablets, USP 45 mg are grey colored, modified capsule shaped, biconvex, coated tablets, debossed with "531" on one side and plain on other side and are supplied as follows:
NDC 68382-531-06 in bottles of 30 tablets with child resistance closure
NDC 68382-531-16 in bottles of 90 tablets with child resistance closure
NDC 68382-531-01 in bottles of 100 tablets with child resistance closure
NDC 68382-531-05 in bottles of 500 tablets
NDC 68382-531-10 in bottles of 1000 tablets
NDC 68382-531-30 in unit-dose blister cartons of 100Â (10 x 10) unit-dose tablets
Minocycline Hydrochloride Extended-release Tablets, USP 55 mg are yellow colored, modified capsule shaped, biconvex, coated tablets, debossed with "550" on one side and plain on other side and are supplied as follows:
NDC 68382-550-06 in bottles of 30 tablets with child resistance closure
NDC 68382-550-16 in bottles of 90 tablets with child resistance closure
NDC 68382-550-01 in bottles of 100 tablets with child resistance closure
NDC 68382-550-05 in bottles of 500 tablets
NDC 68382-550-10 in bottles of 1000 tablets
NDC 68382-550-30 in unit-dose blister cartons of 100Â (10 x 10) unit-dose tablets
Minocycline Hydrochloride Extended-release Tablets, USP 65 mg are blue colored, modified capsule shaped, biconvex, coated tablets, debossed with "532" on one side and plain on other side and are supplied as follows:
NDC 68382-532-06 in bottles of 30 tablets with child resistance closure
NDC 68382-532-16 in bottles of 90 tablets with child resistance closure
NDC 68382-532-01 in bottles of 100 tablets with child resistance closure
NDC 68382-532-05 in bottles of 500 tablets
NDC 68382-532-10 in bottles of 1000 tablets
NDC 68382-532-30 in unit-dose blister cartons of 100Â (10 x 10) unit-dose tablets
Minocycline Hydrochloride Extended-release Tablets, USP 80 mg are whitish blue colored, modified capsule shaped, biconvex, coated tablets, debossed with "551" on one side and plain on other side and are supplied as follows:
NDC 68382-551-06 in bottles of 30 tablets with child resistance closure
NDC 68382-551-16 in bottles of 90 tablets with child resistance closure
NDC 68382-551-01 in bottles of 100 tablets with child resistance closure
NDC 68382-551-05 in bottles of 500 tablets
NDC 68382-551-10 in bottles of 1000 tablets
NDC 68382-551-30 in unit-dose blister cartons of 100Â (10 x 10) unit-dose tablets
Minocycline Hydrochloride Extended-release Tablets, USP 90 mg are light yellow colored, modified capsule shaped, biconvex, coated tablets, debossed with "533" on one side and plain on other side and are supplied as follows:
NDC 68382-533-06 in bottles of 30 tablets with child resistance closure
NDC 68382-533-16 in bottles of 90 tablets with child resistance closure
NDC 68382-533-01 in bottles of 100 tablets with child resistance closure
NDC 68382-533-05 in bottles of 500 tablets
NDC 68382-533-10 in bottles of 1000 tablets
NDC 68382-533-30 in unit-dose blister cartons of 100Â (10 x 10) unit-dose tablets
Minocycline Hydrochloride Extended-release Tablets, USP 105 mg are light blue colored, modified capsule shaped, biconvex, coated tablets, debossed with "552" on one side and plain on other side and are supplied as follows:
NDC 68382-552-06 in bottles of 30 tablets with child resistance closure
NDC 68382-552-16 in bottles of 90 tablets with child resistance closure
NDC 68382-552-01 in bottles of 100 tablets with child resistance closure
NDC 68382-552-05 in bottles of 500 tablets
NDC 68382-552-10 in bottles of 1000 tablets
NDC 68382-552-30 in unit-dose blister cartons of 100Â (10 x 10) unit-dose tablets
Minocycline Hydrochloride Extended-release Tablets, USP 115 mg are green colored, modified capsule shaped, biconvex, coated tablets, debossed with "534" on one side and plain on other side and are supplied as follows:
NDC 68382-534-06 in bottles of 30 tablets with child resistance closure
NDC 68382-534-16 in bottles of 90 tablets with child resistance closure
NDC 68382-534-01 in bottles of 100 tablets with child resistance closure
NDC 68382-534-05 in bottles of 500 tablets
NDC 68382-534-10 in bottles of 1000 tablets
NDC 68382-534-30 in unit-dose blister cartons of 100Â (10 x 10) unit-dose tablets
Minocycline Hydrochloride Extended-release Tablets, USP 135 mg are light pink colored, modified capsule shaped, biconvex, coated tablets, debossed with "535" on one side and plain on other side and are supplied as follows:
NDC 68382-535-06 in bottles of 30 tablets with child resistance closure
NDC 68382-535-16 in bottles of 90 tablets with child resistance closure
NDC 68382-535-01 in bottles of 100 tablets with child resistance closure
NDC 68382-535-05 in bottles of 500 tablets
NDC 68382-535-10 in bottles of 1000 tablets
NDC 68382-535-30 in unit-dose blister cartons of 100Â (10 x 10) unit-dose tablets
Storage
Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature].
Handling
Keep this and all drugs out of the reach of children.
Protect from light, moisture and excessive heat.
Dispense in a tight, light-resistant container as defined in the USP with child-resistant closure.
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17 PATIENT COUNSELING INFORMATION
Advise the patient to read the FDA-approved patient labeling (Patient Information).
Patients taking minocycline hydrochloride extended-release tablets should receive the following information and instructions:
Administration Instructions
- Minocycline hydrochloride extended-release tablets should be taken exactly as directed.
- Advise patients to swallow minocycline extended-release tablets whole and not to chew, crush, or split the tablets [see Dosage and Administration (2)].
Serious Skin/Hypersensitivity Reactions
- Inform patients that serious skin reactions have occurred with the minocycline use in patients with acne. Advise patients to discontinue use of minocycline extended-release tablets and contact their healthcare provider immediately at the first evidence of skin erythema [see Warnings and Precautions (5.1)].
Tooth Discoloration and Enamel Hypoplasia
- Advise patients that minocycline extended-release tablets use in pregnancy may cause permanent tooth discoloration of deciduous teeth. Advise patients to discontinue minocycline extended-release tablets during pregnancy and to inform their healthcare provider right away if they become pregnant during treatment [see Warnings and Precautions (5.2), Use in Specific Populations (8.1)].
- Advise caregivers of pediatric patients that minocycline extended-release tablets use may cause permanent discoloration of deciduous and permanent teeth [see Warnings and Precautions (5.2), Use in Specific Populations (8.4)].
- Advise patients that minocycline use in pregnancy may cause inhibition of fetal bone growth. Advise patients to discontinue minocycline during pregnancy and to inform their healthcare provider right away if they become pregnant during treatment [see Warnings and Precautions (5.3), Use in Specific Populations (8.1)].
Clostridioides difficile-Associated Diarrhea (Antibiotic-Associated Colitis)
- Advise patients that Clostridioides difficile-associated diarrhea (antibiotic-associated colitis) can occur with minocycline therapy, including minocycline extended-release tablets. If patients develop watery or bloody stools, advise patients to seek medical attention [see Warnings and Precautions (5.4)].
- Inform patients about the possibility of hepatotoxicity. Advise patients to seek medical advice if they experience signs or symptoms of hepatotoxicity, including loss of appetite, tiredness, diarrhea, jaundice, bleeding easily, confusion, and sleepiness [see Warnings and Precautions (5.5)].
Central Nervous System Effects
- Inform patients that central nervous system adverse reactions including dizziness or vertigo have been reported with oral minocycline therapy. Caution patients about driving vehicles or using hazardous machinery if they experience such symptoms while on minocycline[see Warnings and Precautions (5.6)].
Idiopathic Intracranial Hypertension
- Inform patients that idiopathic intracranial hypertension can occur with minocycline therapy. Advise patients to seek medical attention if they develop unusual headache, visual symptoms, such as blurred vision, diplopia, and vision loss [see Warnings and Precautions (5.7)].
- Inform patients that autoimmune syndromes, including drug-induced lupus-like syndrome, autoimmune hepatitis, vasculitis, and serum sickness have been observed with tetracycline-class drugs, including minocycline. Symptoms may be manifested by arthralgia, fever, rash, and malaise. Advise patients who experience such symptoms to immediately discontinue minocycline and seek medical help [see Warnings and Precautions (5.8)].
- Inform patients that photosensitivity manifested by an exaggerated sunburn reaction has been observed in some individuals taking tetracyclines, including minocycline. Advise patients to minimize or avoid exposure to natural or artificial sunlight (i.e., tanning beds or UVA/B treatment) while using minocycline. Instruct patients to use sunscreen and wear protective clothing (e.g., hat) over treated areas when exposure to sun cannot be avoided [see Warnings and Precautions (5.10)].
- Inform patients that minocycline may cause discoloration of skin, scars, teeth, or gums [see Warnings and Precautions (5.11)].
- Advise patients that minocycline therapy is not recommended during breast feeding for 4 days after the final dose [see Use in Specific Populations (8.2)].
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
Manufactured by:
Zydus Lifesciences Ltd.,
Ahmedabad, India
Distributed by:
Zydus Pharmaceuticals (USA) Inc.
Pennington, NJ 08534
Rev.: 06/25
-
PATIENT PACKAGE INSERT
Minocycline Hydrochloride Extended-release Tablets
What are minocycline hydrochloride extended-release tablets?Â
Minocycline hydrochloride extended-release tablets are a prescription medicine used to treat pimples and red bumps (non-nodular inflammatory lesions) that happen with moderate to severe acne vulgaris in people 12 years of age and older. Minocycline hydrochloride extended-release tablets are not effective for acne that is not red-looking (not-inflammatory acne).
- safe and effective for the treatment of infections.
- safe and effective in children under 12 years of age.
Who should not take minocycline hydrochloride extended-release tablets?
Do not take minocycline hydrochloride extended-release tablets if you are allergic to any tetracycline medicines. Ask your healthcare provider or pharmacist for a list of these medicines if you are not sure.
Before taking minocycline hydrochloride extended-release tablets, tell your healthcare provider about all of your medical conditions, including if you:
- have kidney problems.
- have liver problems.
- have diarrhea or watery stools.
- have had increased pressure around your brain that may have caused vision problems.
- are pregnant or plan to become pregnant. Minocycline hydrochloride extended-release tablets may harm your unborn baby. Taking minocycline hydrochloride extended-release tablets while you are pregnant may cause serious side effects on the growth of bone and teeth of your baby. Stop taking minocycline hydrochloride extended-release tablets and call your healthcare provider right away if you become pregnant during treatment with minocycline hydrochloride extended-release tablets.
- are breastfeeding or plan to breastfeed. Minocycline hydrochloride passes into your breast milk and may harm your baby. Do not breastfeed during treatment with minocycline hydrochloride extended-release tablets and for 4 days after your final dose.
Tell your healthcare provider about all the other medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
Minocycline hydrochloride extended-release tablets and other medicines may affect each other and can cause serious side effects. Minocycline may affect the way other medicines work, and other medicines may affect how Minocycline hydrochloride extended-release tablets works.
Especially tell your healthcare provider if you take:
- a blood thinner medicine.
- a penicillin antibiotic medicine.
- antacids that contain aluminum, calcium, or magnesium or iron-containing medicines.
- an acne medicine that contains isotretinoin
Ask your healthcare provider or pharmacist if you are not sure if your medicine is one that is listed above. Know the medicines you take. Keep a list of them to show your healthcare provider and pharmacist.
How should I take minocycline hydrochloride extended-release tablets?
- Take minocycline hydrochloride extended-release tablets exactly as your healthcare provider tells you.
- Take minocycline hydrochloride extended-release tablets 1 time per day with or without food. Taking minocycline hydrochloride extended-release tablets with food may lower your chances of getting irritation or ulcers in your esophagus. Your esophagus is the tube that connects your mouth to your stomach.
- Swallow minocycline hydrochloride extended-release tablets whole. Do not chew, crush, or split the tablets.
If you take too much minocycline hydrochloride extended-release tablets, stop taking minocycline hydrochloride extended-release tablet and call your healthcare provider or go to the nearest hospital emergency room, or contact a poison control center right away at 1-800-222-1222.
What should I avoid while taking minocycline hydrochloride extended-release tablets?
- You should not drive or operate dangerous machinery until you know how minocycline hydrochloride extended-release tablet affects you. Minocycline hydrochloride extended-release tablets may cause you to feel dizzy or lightheaded, or have a spinning feeling (vertigo).
- Avoid sunlight or artificial sunlight, such as sunlamps and tanning beds during treatment with minocycline hydrochloride extended-release tablet. Minocycline hydrochloride extended-release tablet can make your skin sensitive to the sun and artificial sunlight and you could get severe sunburn during treatment. Use sunscreen and wear a hat and protective clothing that covers your skin while out in the sunlight during treatment with minocycline hydrochloride extended-release tablet.
What are possible side effects of minocycline hydrochloride extended-release tablets?Â
Minocycline hydrochloride extended-release tablets may cause serious side effects, including:Â
- Serious skin and allergic reactions have happened during treatment with minocycline. Minocycline hydrochloride extended-release tablets may cause serious skin or allergic reactions that may also affect parts of your body such as your liver, lungs, kidneys, and heart. Sometimes these reactions can lead to death. Stop taking minocycline hydrochloride extended-release tablets and call your healthcare provider right away or go to the nearest hospital emergency room if you have any of the following signs or symptoms, including:
â—‹
skin redness, rash, hives, sores in your mouth, or your skin blisters and peels
â—‹
swelling of your face, eyes, lips, tongue, or throat
â—‹
trouble swallowing or breathing
â—‹
blood in your urine
â—‹
fever, yellowing of the skin or the whites of your eyes (jaundice), dark colored urine
â—‹
pain on the right side of the stomach area (abdominal pain)
â—‹
chest pain or abnormal heartbeats
â—‹
swelling in your legs, ankles, and feet
- Permanent tooth discoloration and problems with tooth enamel. Minocycline hydrochloride extended-release tablets may permanently turn a baby or child's teeth yellow-grey-brown during tooth development. Minocycline hydrochloride extended-release tablets may also cause tooth enamel to not develop properly. You should not use minocycline hydrochloride extended-release tablets during tooth development. Tooth development happens in the second and third trimesters of pregnancy, and in children from birth to 8 years of age. See "What should I tell my healthcare provider before taking minocycline hydrochloride extended-release tablets?"
- Slow bone growth. Minocycline hydrochloride extended-release tablets may cause slow bone growth if it is used during the second and third trimesters of pregnancy and if it is used in infants and children up to 8 years of age. Slow bone growth is reversible after stopping treatment with minocycline hydrochloride extended-release tablets.
- Diarrhea (antibiotic associated colitis). Antibiotic associated colitis can happen with most antibiotics, including minocycline hydrochloride extended-release tablets. This type of diarrhea may be caused by an infection (Clostridioides difficile) in your intestines and can be severe and can lead to death. Call your healthcare provider right away if you get watery diarrhea, diarrhea that does not go away, or bloody stools.
- Liver problems. Minocycline hydrochloride extended-release tablets may cause serious liver problems that can lead to death. Stop taking minocycline hydrochloride extended-release tablets and call your healthcare provider right away if you get any of the following symptoms of liver problems:
â—‹
loss of appetite
â—‹
tiredness
â—‹
diarrhea
â—‹
yellowing of your skin or the whites of your eyes (jaundice)
â—‹
unexplained bleeding or bleeding more easily than normal
â—‹
confusion
â—‹
sleepiness
- Central nervous system effects. See "What should I avoid while taking minocycline hydrochloride extended-release tablets?" Central nervous system effects such as light-headedness, dizziness, and a spinning feeling (vertigo) may go away during your treatment with minocycline hydrochloride extended-release tablets or if treatment is stopped.
- Increased pressure around the brain (idiopathic intracranial hypertension). This condition may lead to vision changes and permanent vision loss. You are more likely to get intracranial hypertension if you are a female who can have children, are overweight, and have already had intracranial hypertension. Stop taking minocycline hydrochloride extended-release tablets and tell your healthcare provider right away if you have blurred vision, double vision, vision loss, or unusual headaches.
- Immune system reactions including a lupus-like syndrome, hepatitis, and inflammationof blood or lymph vessels (vasculitis).Using minocycline hydrochloride extended-release tablets for a long time to treat acne may cause immune system reactions. Stop taking m      inocycline hydrochloride extended-release tablets and tell your healthcare provider right away if you get a fever, rash, joint pain, or body weakness.
- Sensitivity to sunlight (photosensitivity). See"What should I avoid while taking minocycline hydrochloride extended-release tablets?"
- Discoloration (tissue hyperpigmentation). Minocycline hydrochloride extended-release tablets may cause darkening of your nails, skin, eyes, teeth, gums, scars, and internal organs.
The most common side effects of minocycline hydrochloride extended-release tablets include:
- headache
- tiredness
- dizziness or spinning feeling
- itching
Your healthcare provider may do blood tests and check you for side effects during treatment with minocycline hydrochloride extended-release tablets and may lower your dose or stop treatment if you develop certain side effects.
These are not all of the possible side effects of minocycline hydrochloride extended-release tablets.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. You may also report side effects to MedicalAffairs@ zydususa.com at 1-877-993-8779.
How should I store minocycline hydrochloride extended-release tablets?
- Store minocycline hydrochloride extended-release tablets between 59ºF to 86ºF (15ºC to 30ºC).
- Keep minocycline hydrochloride extended-release tablets in the container that it comes in and keep the container tightly closed.
- Keep minocycline hydrochloride extended-release tablets dry.
Keep minocycline hydrochloride extended-release tablets and all medicines out of the reach of children.
General information about the safe and effective use of minocycline hydrochloride extended-release tabletsÂ
Medicines are sometimes prescribed for purposes other than those listed in the Patient Information leaflet. Do not use minocycline hydrochloride extended-release tablets for a condition for which it was not prescribed. Do not give minocycline hydrochloride extended-release tablets to other people, even if they have the same symptoms you have. It may harm them. You can ask your pharmacist or healthcare provider for information about minocycline hydrochloride extended-release tablets that is written for health professionals.
Please address medical inquiries to, (MedicalAffairs@zydususa.com) Tel.: 1-877-993-8779.
What are the ingredients in minocycline hydrochloride extended-release tablets?
Active ingredient: minocycline hydrochloride, USP
Inactive ingredients: colloidal silicon dioxide, hypromellose, lactose monohydrate, magnesium stearate, polyethylene glycol (55 mg, 65 mg, 80 mg, 90 mg, 105 mg, 115 mg and 135 mg only), titanium dioxide and triacetin.
Additionally, the 45 mg tablets contain ferric oxide black and ferric oxide yellow; the 55 mg tablets contain ferric oxide red and ferric oxide yellow; the 65 mg tablets contain FD & C blue #2 aluminum lake; the 80 mg tablets contain FD & C blue #2 aluminum lake and FD & C red #40 aluminum lake; the 90 mg tablets contain D & C yellow #10 aluminum lake, ferric oxide red and ferric oxide yellow; the 105 mg tablets contain FD & C blue #2 aluminum lake and FD & C red #40 aluminum lake; the 115 mg tablets contain FD & C blue #2 aluminum lake and ferric oxide yellow; the 135 mg tablets contain D & C red #27 aluminum lake, D & C yellow #10 aluminum lake and FD & C blue #2 aluminum lake.
Brands mentioned are trademarks of their respective owners.
Manufactured by:
Zydus Lifesciences Ltd.,
Ahmedabad, India
Distributed by:
Zydus Pharmaceuticals (USA) Inc.
Pennington, NJ 08534
This Patient Information has been approved by the U.S. Food and Drug Administration
Rev.: 06/25
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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC 68382-531-01 in bottle of 100 Tablets
Minocycline Hydrochloride Extended-release Tablets, USP 45 mg
Rx only
100 TABLETS
ZYDUS
NDC 68382-550-01 in bottle of 100 Tablets
Minocycline Hydrochloride Extended-release Tablets, USP 55 mg
Rx only
100 TABLETS
ZYDUS
NDC 68382-532-01 in bottle of 100 Tablets
Minocycline Hydrochloride Extended-release Tablets, USP 65 mg
Rx only
100 TABLETS
ZYDUS
NDC 68382-551-01 in bottle of 100 Tablets
Minocycline Hydrochloride Extended-release Tablets, USP 80 mg
Rx only
100 TABLETS
ZYDUS
NDC 68382-533-01 in bottle of 100 Tablets
Minocycline Hydrochloride Extended-release Tablets, USP 90 mg
Rx only
100 TABLETS
ZYDUS
NDC 68382-552-01 in bottle of 100 Tablets
Minocycline Hydrochloride Extended-release Tablets, USP 105 mg
Rx only
100 TABLETS
ZYDUS
NDC 68382-534-01 in bottle of 100 Tablets
Minocycline Hydrochloride Extended-release Tablets, USP 115 mg
Rx only
100 TABLETS
ZYDUS
NDC 68382-535-01 in bottle of 100 Tablets
Minocycline Hydrochloride Extended-release Tablets, USP 135 mg
Rx only
100 TABLETS
ZYDUS
-
INGREDIENTS AND APPEARANCE
MINOCYCLINE HYDROCHLORIDEÂ
minocycline hydrochloride tablet, extended releaseProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68382-531 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOCYCLINE HYDROCHLORIDE (UNII: 0020414E5U) (MINOCYCLINE - UNII:FYY3R43WGO) MINOCYCLINE 45 mg Inactive Ingredients Ingredient Name Strength FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  FERROSOFERRIC OXIDE (UNII: XM0M87F357)  HYPROMELLOSES (UNII: 3NXW29V3WO)  LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  MAGNESIUM STEARATE (UNII: 70097M6I30)  SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  TRIACETIN (UNII: XHX3C3X673)  Product Characteristics Color GRAY (gray) Score no score Shape CAPSULE (capsule) Size 9mm Flavor Imprint Code 531 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68382-531-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 2 NDC:68382-531-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 3 NDC:68382-531-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 4 NDC:68382-531-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 5 NDC:68382-531-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 6 NDC:68382-531-30 10 in 1 CARTON 03/07/2018 6 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA203553 03/07/2018 MINOCYCLINE HYDROCHLORIDEÂ
minocycline hydrochloride tablet, extended releaseProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68382-550 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOCYCLINE HYDROCHLORIDE (UNII: 0020414E5U) (MINOCYCLINE - UNII:FYY3R43WGO) MINOCYCLINE 55 mg Inactive Ingredients Ingredient Name Strength FERRIC OXIDE RED (UNII: 1K09F3G675)  FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  HYPROMELLOSES (UNII: 3NXW29V3WO)  LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  MAGNESIUM STEARATE (UNII: 70097M6I30)  POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  TRIACETIN (UNII: XHX3C3X673)  Product Characteristics Color YELLOW Score no score Shape CAPSULE (capsule) Size 10mm Flavor Imprint Code 550 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68382-550-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 2 NDC:68382-550-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 3 NDC:68382-550-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 4 NDC:68382-550-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 5 NDC:68382-550-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 6 NDC:68382-550-30 10 in 1 CARTON 06/12/2025 6 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA203553 06/12/2025 MINOCYCLINE HYDROCHLORIDEÂ
minocycline hydrochloride tablet, extended releaseProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68382-532 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOCYCLINE HYDROCHLORIDE (UNII: 0020414E5U) (MINOCYCLINE - UNII:FYY3R43WGO) MINOCYCLINE 65 mg Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  HYPROMELLOSES (UNII: 3NXW29V3WO)  LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  MAGNESIUM STEARATE (UNII: 70097M6I30)  POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  TRIACETIN (UNII: XHX3C3X673)  Product Characteristics Color BLUE Score no score Shape CAPSULE (capsule) Size 11mm Flavor Imprint Code 532 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68382-532-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 2 NDC:68382-532-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 3 NDC:68382-532-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 4 NDC:68382-532-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 5 NDC:68382-532-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 6 NDC:68382-532-30 10 in 1 CARTON 06/12/2025 6 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA203553 06/12/2025 MINOCYCLINE HYDROCHLORIDEÂ
minocycline hydrochloride tablet, extended releaseProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68382-551 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOCYCLINE HYDROCHLORIDE (UNII: 0020414E5U) (MINOCYCLINE - UNII:FYY3R43WGO) MINOCYCLINE 80 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  FD&C RED NO. 40 (UNII: WZB9127XOA)  HYPROMELLOSES (UNII: 3NXW29V3WO)  LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  MAGNESIUM STEARATE (UNII: 70097M6I30)  POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  TRIACETIN (UNII: XHX3C3X673)  Product Characteristics Color BLUE (whitish blue) Score no score Shape CAPSULE (capsule) Size 12mm Flavor Imprint Code 551 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68382-551-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 2 NDC:68382-551-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 3 NDC:68382-551-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 4 NDC:68382-551-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 5 NDC:68382-551-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 6 NDC:68382-551-30 10 in 1 CARTON 03/07/2018 6 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA203553 03/07/2018 MINOCYCLINE HYDROCHLORIDEÂ
minocycline hydrochloride tablet, extended releaseProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68382-533 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOCYCLINE HYDROCHLORIDE (UNII: 0020414E5U) (MINOCYCLINE - UNII:FYY3R43WGO) MINOCYCLINE 90 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  FERRIC OXIDE RED (UNII: 1K09F3G675)  FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  HYPROMELLOSES (UNII: 3NXW29V3WO)  LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  MAGNESIUM STEARATE (UNII: 70097M6I30)  POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  TRIACETIN (UNII: XHX3C3X673)  Product Characteristics Color YELLOW (light yellow) Score no score Shape CAPSULE (capsule) Size 13mm Flavor Imprint Code 533 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68382-533-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 2 NDC:68382-533-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 3 NDC:68382-533-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 4 NDC:68382-533-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 5 NDC:68382-533-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 6 NDC:68382-533-30 10 in 1 CARTON 03/07/2018 6 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA203553 03/07/2018 MINOCYCLINE HYDROCHLORIDEÂ
minocycline hydrochloride tablet, extended releaseProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68382-552 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOCYCLINE HYDROCHLORIDE (UNII: 0020414E5U) (MINOCYCLINE - UNII:FYY3R43WGO) MINOCYCLINE 105 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  FD&C RED NO. 40 (UNII: WZB9127XOA)  HYPROMELLOSES (UNII: 3NXW29V3WO)  LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  MAGNESIUM STEARATE (UNII: 70097M6I30)  POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  TRIACETIN (UNII: XHX3C3X673)  Product Characteristics Color BLUE (light blue) Score no score Shape CAPSULE (capsule) Size 14mm Flavor Imprint Code 552 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68382-552-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 2 NDC:68382-552-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 3 NDC:68382-552-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 4 NDC:68382-552-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 5 NDC:68382-552-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 6 NDC:68382-552-30 10 in 1 CARTON 03/07/2018 6 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA203553 03/07/2018 MINOCYCLINE HYDROCHLORIDEÂ
minocycline hydrochloride tablet, extended releaseProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68382-534 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOCYCLINE HYDROCHLORIDE (UNII: 0020414E5U) (MINOCYCLINE - UNII:FYY3R43WGO) MINOCYCLINE 115 mg Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  HYPROMELLOSES (UNII: 3NXW29V3WO)  LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  MAGNESIUM STEARATE (UNII: 70097M6I30)  POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  TRIACETIN (UNII: XHX3C3X673)  Product Characteristics Color GREEN (green) Score no score Shape CAPSULE (capsule) Size 16mm Flavor Imprint Code 534 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68382-534-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 2 NDC:68382-534-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 3 NDC:68382-534-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 4 NDC:68382-534-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 5 NDC:68382-534-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 06/12/2025 6 NDC:68382-534-30 10 in 1 CARTON 06/12/2025 6 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA203553 06/12/2025 MINOCYCLINE HYDROCHLORIDEÂ
minocycline hydrochloride tablet, extended releaseProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68382-535 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MINOCYCLINE HYDROCHLORIDE (UNII: 0020414E5U) (MINOCYCLINE - UNII:FYY3R43WGO) MINOCYCLINE 135 mg Inactive Ingredients Ingredient Name Strength D&C RED NO. 27 (UNII: 2LRS185U6K)  D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  HYPROMELLOSES (UNII: 3NXW29V3WO)  LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  MAGNESIUM STEARATE (UNII: 70097M6I30)  POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  TRIACETIN (UNII: XHX3C3X673)  Product Characteristics Color PINK (light pink) Score no score Shape CAPSULE (capsule) Size 16mm Flavor Imprint Code 535 Contains     Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68382-535-06 30 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 2 NDC:68382-535-16 90 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 3 NDC:68382-535-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 4 NDC:68382-535-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 5 NDC:68382-535-10 1000 in 1 BOTTLE; Type 0: Not a Combination Product 03/07/2018 6 NDC:68382-535-30 10 in 1 CARTON 03/07/2018 6 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA203553 03/07/2018 Labeler - Zydus Pharmaceuticals (USA) Inc. (156861945)