Label: DEXAMETHASONE SODIUM PHOSPHATE injection, solution

  • NDC Code(s): 25021-052-01, 25021-052-05, 25021-053-01
  • Packager: Sagent Pharmaceuticals
  • Category: HUMAN PRESCRIPTION DRUG LABEL

Drug Label Information

Updated December 10, 2024

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  • SPL UNCLASSIFIED SECTION

    SAGENT®
    Rx only

  • DESCRIPTION

    Dexamethasone Sodium Phosphate Injection, USP, is a water-soluble inorganic ester of dexamethasone which produces a rapid response even when injected intramuscularly.

    Dexamethasone Sodium Phosphate, USP C22H28FNa2O8P, has a molecular weight of 516.4 and chemically is 9-fluoro-11β, 17, 21-trihydroxy-16α-methylpregna-1,4-diene-3,20-dione, 21-(dihydrogen phosphate) disodium salt.

    It occurs as a white to practically white powder, is exceedingly hygroscopic, is soluble in water and its solutions have a pH between 7.5 and 9.5. It has the following structural formula:

    Figure

    Dexamethasone Sodium Phosphate Injection, USP is available in 4 mg per mL and 10 mg per mL concentrations.

    Each mL of Dexamethasone Sodium Phosphate Injection USP, 4 mg per mL contains dexamethasone sodium phosphate, USP equivalent to 4 mg of dexamethasone phosphate; 11 mg sodium citrate anhydrous; 1 mg sodium sulfite; 10 mg benzyl alcohol (preservative); water for injection, q.s. NaOH and/or citric acid monohydrate to adjust pH if necessary. pH: 7.0 to 8.5.

    Each mL of Dexamethasone Sodium Phosphate Injection, USP, 10 mg per mL (Preservative Free) contains dexamethasone sodium phosphate, USP equivalent to 10 mg dexamethasone phosphate; 24.75 mg sodium citrate, dihydrate; and Water for Injection, q.s. pH adjusted with citric acid or sodium hydroxide, if necessary. pH: 7.0 to 8.5.

  • CLINICAL PHARMACOLOGY

    Naturally occurring glucocorticoids (hydrocortisone), which also have salt-retaining properties, are used as replacement therapy in adrenocortical deficiency states. Their synthetic analogs are primarily used for their potent anti-inflammatory effects in disorders of many organ systems.

    Glucocorticoids cause profound and varied metabolic effects. In addition, they modify the body's immune responses to diverse stimuli.

  • INDICATIONS AND USAGE

    A. Intravenous or Intramuscular Administration

    When oral therapy is not feasible and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, those products labeled for intravenous or intramuscular use are indicated as follows:

    1. Endocrine Disorders

     
    Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance).
     
    Acute adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; mineralocorticoid supplementation may be necessary, particularly when synthetic analogs are used).
     
    Preoperatively, and in the event of serious trauma or illness, in patients with known adrenal insufficiency or when adrenocortical reserve is doubtful.
     
    Shock unresponsive to conventional therapy if adrenocortical insufficiency exists or is suspected.
     
    Congenital adrenal hyperplasia.
     
    Nonsuppurative thyroiditis.
     
    Hypercalcemia associated with cancer.

    2. Rheumatic Disorders

     
    As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in:
     
    Post-traumatic osteoarthritis.
     
    Synovitis of osteoarthritis.
     
    Rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy).
     
    Acute and subacute bursitis.
     
    Epicondylitis.
     
    Acute nonspecific tenosynovitis.
     
    Acute gouty arthritis.
     
    Psoriatic arthritis.
     
    Ankylosing spondylitis.

    3. Collagen Diseases

     
    During an exacerbation or as maintenance therapy in selected cases of:
     
    Systemic lupus erythematosus.
     
    Acute rheumatic carditis.

    4. Dermatologic Diseases

     
    Pemphigus.
     
    Severe erythema multiforme (Stevens-Johnson syndrome).
     
    Exfoliative dermatitis.
     
    Bullous dermatitis herpetiformis.
     
    Severe seborrheic dermatitis.
     
    Severe psoriasis.
     
    Mycosis fungoides.

    5. Allergic States

     
    Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in:
     
    Bronchial asthma.
     
    Contact dermatitis.
     
    Atopic dermatitis.
     
    Serum sickness.
     
    Seasonal or perennial allergic rhinitis.
     
    Drug hypersensitivity reactions.
     
    Urticarial transfusion reactions.
     
    Acute noninfectious laryngeal edema (epinephrine is the drug of first choice).

    6. Ophthalmic Diseases

     
    Severe acute and chronic allergic and inflammatory processes involving the eye, such as:
     
    Herpes zoster ophthalmicus.
     
    Iritis, iridocyclitis.
     
    Chorioretinitis.
     
    Diffuse posterior uveitis and choroiditis.
     
    Optic neuritis.
     
    Sympathetic ophthalmia.
     
    Anterior segment inflammation.
     
    Allergic conjunctivitis.
     
    Allergic corneal marginal ulcers.
     
    Keratitis.

    7. Gastrointestinal Diseases

     
    To tide the patient over a critical period of the disease in:
     
    Ulcerative colitis (systemic therapy).
     
    Regional enteritis (systemic therapy).

    8. Respiratory Diseases

     
    Symptomatic sarcoidosis.
     
    Berylliosis.
     
    Fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate anti-tuberculosis chemotherapy.
     
    Loeffler's syndrome not manageable by other means.
     
    Aspiration pneumonitis.

    9. Hematologic Disorders

     
    Acquired (autoimmune) hemolytic anemia.
     
    Idiopathic thrombocytopenic purpura in adults (I.V. only; I.M. administration is contraindicated).
     
    Secondary thrombocytopenia in adults.
     
    Erythroblastopenia (RBC anemia).
     
    Congenital (erythroid) hypoplastic anemia.

    10. Neoplastic Diseases

     
    For palliative management of:
     
    Leukemias and lymphomas in adults.
     
    Acute leukemia of childhood.

    11. Edematous States

     
    To induce diuresis or remission of proteinuria in the nephrotic syndrome, without uremia, of the idiopathic type or that due to lupus erythematosus.

    12. Nervous System

     
    Acute exacerbations of multiple sclerosis.

    13. Miscellaneous

     
    Tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate anti-tuberculosis chemotherapy.
     
    Trichinosis with neurologic or myocardial involvement.
     
    Diagnostic testing of adrenocortical hyperfunction.
     
    Cerebral edema of diverse etiologies in conjunction with adequate neurological evaluation and management.

    B. Intra-Articular or Soft Tissue Administration

    When the strength and dosage form of the drug lend the preparation to the treatment of the condition, those products labeled for intra-articular or soft tissue administration are indicated as adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in:

     
    Synovitis of osteoarthritis.
     
    Rheumatoid arthritis.
     
    Acute and subacute bursitis.
     
    Acute gouty arthritis.
     
    Epicondylitis.
     
    Acute nonspecific tenosynovitis.
     
    Post-traumatic osteoarthritis.

    C. Intralesional Administration

    When the strength and dosage form of the drug lend the preparation to the treatment of the condition, those products labeled for intralesional administration are indicated for:

     
    Keloids.
     
    Localized hypertrophic, infiltrated, inflammatory lesions of: lichen planus, psoriatic plaques, granuloma annulare, and lichen simplex chronicus (neurodermatitis).
     
    Discoid lupus erythematosus.
     
    Necrobiosis lipoidica diabeticorum.
     
    Alopecia areata.
     
    They also may be useful in cystic tumors of an aponeurosis tendon (ganglia).
  • CONTRAINDICATIONS

    Systemic fungal infections.

  • WARNINGS

    Serious Neurologic Adverse Reactions with Epidural Administration

    Serious neurologic events, some resulting in death, have been reported with epidural injection of corticosteroids. Specific events reported include, but are not limited to, spinal cord infarction, paraplegia, quadriplegia, cortical blindness, and stroke. These serious neurologic events have been reported with and without use of fluoroscopy. The safety and effectiveness of epidural administration of corticosteroids have not been established, and corticosteroids are not approved for this use.

    In patients on corticosteroid therapy subject to any unusual stress, increased dosage of rapidly acting corticosteroids before, during and after the stressful situation is indicated.

    Prolonged use of corticosteroids may produce posterior subcapsular cataracts, glaucoma with possible damage to the optic nerves, and may enhance the establishment of secondary ocular infections due to fungi or viruses.

    Immunosuppression and Increased Risk of Infection

    Corticosteroids, including dexamethasone sodium phosphate injection, suppress the immune system and increase the risk of infection with any pathogen, including viral, bacterial, fungal, protozoan, or helminthic pathogens. Corticosteroids can:

    • Reduce resistance to new infections
    • Exacerbate existing infections
    • Increase the risk of disseminated infections
    • Increase the risk of reactivation or exacerbation of latent infections
    • Mask some signs of infection

    Corticosteroid-associated infections can be mild but can be severe and at times fatal. The rate of infectious complications increases with increasing corticosteroid dosages.

    Monitor for the development of infection and consider dexamethasone sodium phosphate injection withdrawal or dosage reduction as needed.

    Do not administer dexamethasone sodium phosphate injection by an intraarticular, intrabursal, intratendinous, or intralesional route in the presence of acute local infection.

    Tuberculosis

    If dexamethasone sodium phosphate injection is used to treat a condition in patients with latent tuberculosis or tuberculin reactivity, reactivation of the disease may occur. Closely monitor such patients for reactivation. During prolonged dexamethasone sodium phosphate injection therapy, patients with latent tuberculosis or tuberculin reactivity should receive chemoprophylaxis.

    Varicella Zoster and Measles Viral Infections

    Varicella and measles can have a serious or even fatal course in non-immune patients taking corticosteroids, including dexamethasone sodium phosphate injection. In corticosteroid-treated patients who have not had these diseases or are non-immune, particular care should be taken to avoid exposure to varicella and measles:

    • If a dexamethasone sodium phosphate-treated patient is exposed to varicella, prophylaxis with varicella zoster immune globulin (VZIG) may be indicated. If varicella develops, treatment with antiviral agents may be considered.
    • If a dexamethasone sodium phosphate-treated patient is exposed to measles, prophylaxis with immunoglobulin (IG) may be indicated.

    Hepatitis B Virus Reactivation

    Hepatitis B virus reactivation can occur in patients who are hepatitis B carriers treated with immunosuppressive dosages of corticosteroids, including dexamethasone sodium phosphate injection. Reactivation can also occur infrequently in corticosteroid-treated patients who appear to have resolved hepatitis B infection.

    Screen patients for hepatitis B infection before initiating immunosuppressive (e.g., prolonged) treatment with dexamethasone sodium phosphate injection. For patients who show evidence of hepatitis B infection, recommend consultation with physicians with expertise in managing hepatitis B regarding monitoring and consideration for hepatitis B antiviral therapy.

    Fungal Infections

    Corticosteroids, including dexamethasone sodium phosphate injection, may exacerbate systemic fungal infections; therefore, avoid dexamethasone sodium phosphate injection use in the presence of such infections unless dexamethasone sodium phosphate injection is needed to control drug reactions. For patients on chronic dexamethasone sodium phosphate injection therapy who develop systemic fungal infections, dexamethasone sodium phosphate injection withdrawal or dosage reduction is recommended.

    Amebiasis

    Corticosteroids, including dexamethasone sodium phosphate injection, may activate latent amebiasis. Therefore, it is recommended that latent amebiasis or active amebiasis be ruled out before initiating dexamethasone sodium phosphate injection in patients who have spent time in the tropics or patients with unexplained diarrhea.

    Strongyloides Infestation

    Corticosteroids, including dexamethasone sodium phosphate injection, should be used with great care in patients with known or suspected Strongyloides (threadworm) infestation. In such patients, corticosteroid-induced immunosuppression may lead to Strongyloides hyperinfection and dissemination with widespread larval migration, often accompanied by severe enterocolitis and potentially fatal gram-negative septicemia.

    Cerebral Malaria

    Avoid corticosteroids, including dexamethasone sodium phosphate injection, in patients with cerebral malaria.

    Kaposi's Sarcoma

    Kaposi's sarcoma has been reported to occur in patients receiving corticosteroid therapy, most often for chronic conditions. Discontinuation of corticosteroids may result in clinical improvement of Kaposi's sarcoma.

    Usage in Pregnancy

    Since adequate human reproduction studies have not been done with corticosteroids, use of these drugs in pregnancy, nursing mothers or women of childbearing potential requires that the possible benefits of the drug be weighed against the potential hazards to the mother and embryo or fetus. Infants born of mothers who have received substantial doses of corticosteroids during pregnancy should be carefully observed for signs of hypoadrenalism.

    Average and large doses of cortisone or hydrocortisone can cause elevation of blood pressure, salt and water retention, and increased excretion of potassium. These effects are less likely to occur with the synthetic derivatives except when used in large doses. Patients with a stressed myocardium should be observed carefully and the drug administered slowly since premature ventricular contractions may occur with rapid administration. Dietary salt restriction and potassium supplementation may be necessary. All corticosteroids increase calcium excretion.

    While on corticosteroid therapy patients should not be vaccinated against smallpox. Other immunization procedures should not be undertaken in patients who are on corticosteroids, especially in high doses, because of possible hazards of neurological complications and lack of antibody response.

    Because rare instances of anaphylactoid reactions have occurred in patients receiving parenteral corticosteroid therapy, appropriate precautionary measures should be taken prior to administration, especially when the patient has a history of allergy to any drug.

    Dexamethasone sodium phosphate injection, 4 mg per mL contains sodium sulfite, a sulfite that may cause allergic type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in nonasthmatic people.

  • PRECAUTIONS

    Drug-induced secondary adrenocortical insufficiency may be minimized by gradual reduction of dosage. This type of relative insufficiency may persist for months after discontinuation of therapy; therefore, in any situation of stress occurring during that period, hormone therapy should be reinstituted. Since mineralocorticoid secretion may be impaired, salt and/or a mineralocorticoid should be administered concurrently.

    There is an enhanced effect of corticosteroids in patients with hypothyroidism and in those with cirrhosis.

    Corticosteroids should be used cautiously in patients with ocular herpes simplex for fear of corneal perforation.

    The lowest possible dose of corticosteroid should be used to control the condition under treatment, and when reduction in dosage is possible, the reduction must be gradual.

    Psychic derangements may appear when corticosteroids are used ranging from euphoria, insomnia, mood swings, personality changes, and severe depression to frank psychotic manifestations. Also, existing emotional instability or psychotic tendencies may be aggravated by corticosteroids.

    Aspirin should be used cautiously in conjunction with corticosteroids in hypoprothrombinemia.

    Steroids should be used with caution in nonspecific ulcerative colitis, if there is a probability of impending perforation, abscess or other pyogenic infection, also in diverticulitis, fresh intestinal anastomoses, active or latent peptic ulcer, renal insufficiency, hypertension, osteoporosis, and myasthenia gravis.

    Growth and development of infants and children on prolonged corticosteroid therapy should be carefully followed.

    Patients who are on immunosuppressant doses of corticosteroids should be warned to avoid exposure to chickenpox or measles and, if exposed, to obtain medical advice.

    Intra-articular injection of a corticosteroid may produce systemic as well as local effects.

    Appropriate examination of any joint fluid present is necessary to exclude a septic process.

    A marked increase in pain accompanied by local swelling, further restriction of joint motion, fever, and malaise are suggestive of septic arthritis. If this complication occurs and the diagnosis of sepsis is confirmed, appropriate antimicrobial therapy should be instituted.

    Local injection of a steroid into a previously infected joint is to be avoided. Corticosteroids should not be injected into unstable joints.

    Although controlled clinical trials have shown corticosteroids to be effective in speeding the resolution of acute exacerbations of multiple sclerosis they do not show that they affect the ultimate outcome or natural history of the disease. The studies do show that relatively high doses of corticosteroids are necessary to demonstrate a significant effect. (see DOSAGE AND ADMINISTRATION Section).

    Since complications of treatment with glucocorticoids are dependent on the size of the dose and the duration of treatment a risk/benefit decision must be made in each individual case as to dose and duration of treatment and as to whether daily or intermittent therapy should be used.

  • ADVERSE REACTIONS

    Fluid and electrolyte disturbances:

     
    Sodium retention
     
    Fluid retention
     
    Congestive heart failure in susceptible patients
     
    Potassium loss
     
    Hypokalemic alkalosis
     
    Hypertension

    Musculoskeletal:

     
    Muscle weakness
     
    Steroid myopathy
     
    Loss of muscle mass
     
    Osteoporosis
     
    Vertebral compression fractures
     
    Aseptic necrosis of femoral and humeral heads
     
    Pathologic fracture of long bones

    Gastrointestinal:

     
    Peptic ulcer with possible subsequent perforation and hemorrhage
     
    Pancreatitis
     
    Abdominal distention
     
    Ulcerative esophagitis

    Dermatological:

     
    Impaired wound healing
     
    Thin fragile skin
     
    Facial erythema
     
    Increased sweating
     
    May suppress reactions to skin tests
     
    Petechiae and ecchymoses

    Neurological:

     
    Convulsions
     
    Increased intracranial pressure with papilledema (pseudotumor cerebri) usually after treatment
     
    Vertigo
     
    Headache

    Ophthalmic:

     
    Posterior subcapsular cataracts
     
    Increased intraocular pressure
     
    Glaucoma

    Endocrine:

     
    Menstrual irregularities
     
    Development of cushingoid state
     
    Suppression of growth in children
     
    Secondary adrenocortical and pituitary unresponsiveness, particularly in times of stress, as in trauma, surgery, or illness
     
    Decreased carbohydrate tolerance
     
    Manifestations of latent diabetes mellitus
     
    Increased requirements for insulin or oral hypoglycemic agents in diabetics

    Metabolic:

     
    Negative nitrogen balance due to protein catabolism

    Miscellaneous:

     
    Hyperpigmentation or hypopigmentation
     
    Subcutaneous and cutaneous atrophy
     
    Sterile abscess
     
    Post-injection flare, following intra-articular use
     
    Charcot-like arthropathy
     
    Itching, burning, tingling in the ano-genital region

    To report SUSPECTED ADVERSE REACTIONS, contact Sagent Pharmaceuticals at 1-866-625-1618 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

  • DOSAGE AND ADMINISTRATION

    A. Intravenous or Intramuscular Administration

    The initial dosage of dexamethasone sodium phosphate injection may vary from 0.50 mg/day to 9.0 mg/day depending on the specific disease entity being treated. In situations of less severity, lower doses will generally suffice while in selected patients higher initial doses may be required. Usually the parenteral dosage ranges are one-third to one-half the oral dose given every 12 hours. However, in certain overwhelming, acute, life-threatening situations, administration of dosages exceeding the usual dosages may be justified and may be in multiples of the oral dosages.

    For the treatment of unresponsive shock high pharmacologic doses of this product are currently recommended. Reported regimens range from 1 to 6 mg/kg of body weight as a single intravenous injection to 40 mg initially followed by repeat intravenous injection every 2 to 6 hours while shock persists.

    For the treatment of cerebral edema in adults an initial intravenous dose of 10 mg is recommended followed by 4 mg intramuscularly every six hours until maximum response has been noted. This regimen may be continued for several days postoperatively in patients requiring brain surgery. Oral dexamethasone, 1 to 3 mg t.i.d., should be given as soon as possible and dosage tapered off over a period of five to seven days. Nonoperative cases may require continuous therapy to remain free of symptoms of increased intracranial pressure. The smallest effective dose should be used in children, preferably orally. This may approximate 0.2 mg/kg/24 hours in divided doses.

    In treatment of acute exacerbations of multiple sclerosis daily doses of 200 mg of prednisolone for a week followed by 80 mg every other day or 4 to 8 mg dexamethasone every other day for 1 month have been shown to be effective.

    The initial dosage should be maintained or adjusted until a satisfactory response is noted. If after a reasonable period of time there is a lack of satisfactory clinical response, dexamethasone sodium phosphate injection should be discontinued and the patient transferred to other appropriate therapy. It should be emphasized that dosage requirements are variable and must be individualized on the basis of the disease under treatment and the response of the patient.

    After a favorable response is noted, the proper maintenance dosage should be determined by decreasing the initial drug dosage in small decrements at appropriate time intervals until the lowest dosage which will maintain an adequate clinical response is reached. It should be kept in mind that constant monitoring is needed in regard to drug dosage. Included in the situations which may make dosage adjustments necessary are changes in clinical status secondary to remissions or exacerbations in the disease process, the patient's individual drug responsiveness and the effect of patient exposure to stressful situations not directly related to the disease entity under treatment. In this later situation it may be necessary to increase the dosage of dexamethasone sodium phosphate injection for a period of time consistent with the patient's condition. If after a long-term therapy the drug is to be stopped, it is recommended that it be withdrawn gradually rather than abruptly.

    B. Intra-Articular, Soft Tissue or Intralesional Administration.

    The dose for intrasynovial administration is usually 2 to 4 mg for large joints and 0.8 to 1 mg for small joints. For soft tissue and bursal injections a dose of 2 to 4 mg is recommended. Ganglia require a dose of 1 to 2 mg. A dose of 0.4 to 1 mg is used for injection into tendon sheaths. Injection into intervertebral joints should not be attempted at any time and hip joint injection cannot be recommended as an office procedure.

    Intrasynovial and soft tissue injections should be employed only when affected areas are limited to 1 or 2 sites. It should be remembered that corticoids provide palliation only and that other conventional or curative methods of therapy should be employed when indicated.

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

    Frequency of injection usually ranges from once every 3 to 5 days to once every 2 to 3 weeks. Frequent intra-articular injection may cause damage to joint tissue.

  • HOW SUPPLIED

    Dexamethasone Sodium Phosphate Injection USP, is a sterile, clear colorless to almost colorless solution free from foreign visible particles is supplied as:

    NDCDexamethasone Sodium Phosphate Injection USPPackage Factor
    (4 mg per mL)
    25021-052-01 4 mg per mL Single-Dose Vial 25 vials per carton
    25021-052-05 20 mg per 5 mL Multi-Dose Vial 25 vials per carton
     
    NDCDexamethasone Sodium Phosphate Injection USPPackage Factor
    (Preservative Free)
    25021-053-01 10 mg per mL Single-Dose Vial 25 vials per carton

    Storage Conditions

    Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature.]

    Protect from light. Retain in carton until time of use.

    Single dose vials - Discard unused portion.

    Sterile, Nonpyrogenic.
    The container closure is not made with natural rubber latex.

    SAGENT® Mfd. for SAGENT Pharmaceuticals
    Schaumburg, IL 60195 (USA)
    Made in India
    ©2024 Sagent Pharmaceuticals

    July 2024

    Sagent Pharmaceuticals®

  • PRINCIPAL DISPLAY PANEL

    PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Vial Label

    NDC 25021-052-01

    Rx only

    Dexamethasone Sodium Phosphate Injection, USP

    4 mg per mL

    (Dexamethasone Phosphate Equivalent)

    For Intravenous or Intramuscular Use

    1 mL Single-Dose Vial

    PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Vial Label
  • PRINCIPAL DISPLAY PANEL

    PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Vial Label

    NDC 25021-052-05

    Rx only

    Dexamethasone Sodium Phosphate Injection, USP

    20 mg per 5 mL

    (4 mg per mL)

    (Dexamethasone Phosphate Equivalent)

    For Intravenous or Intramuscular Use

    5 mL Single-Dose Vial

    PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Vial Label
  • PRINCIPAL DISPLAY PANEL

    PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Vial Label

    NDC 25021-053-01

    Rx only

    Dexamethasone Sodium Phosphate Injection, USP

    10 mg per mL

    (Dexamethasone Phosphate Equivalent)

    For Intravenous or Intramuscular Use

    1 mL Single-Dose Vial

    PACKAGE LABEL – PRINCIPAL DISPLAY PANEL – Vial Label
  • INGREDIENTS AND APPEARANCE
    DEXAMETHASONE SODIUM PHOSPHATE 
    dexamethasone sodium phosphate injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:25021-052
    Route of AdministrationINTRAVENOUS, INTRAMUSCULAR, INTRA-ARTICULAR, SOFT TISSUE, INTRALESIONAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Dexamethasone Sodium Phosphate (UNII: AI9376Y64P) (Dexamethasone - UNII:7S5I7G3JQL) Dexamethasone Phosphate4 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Anhydrous Trisodium Citrate (UNII: RS7A450LGA)  
    Sodium Sulfite (UNII: VTK01UQK3G)  
    Benzyl Alcohol (UNII: LKG8494WBH)  
    Water (UNII: 059QF0KO0R)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:25021-052-0125 in 1 CARTON12/01/2024
    11 mL in 1 VIAL; Type 0: Not a Combination Product
    2NDC:25021-052-0525 in 1 CARTON12/01/2024
    25 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21565412/01/2024
    DEXAMETHASONE SODIUM PHOSPHATE 
    dexamethasone sodium phosphate injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:25021-053
    Route of AdministrationINTRAVENOUS, INTRAMUSCULAR, INTRA-ARTICULAR, SOFT TISSUE, INTRALESIONAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Dexamethasone Sodium Phosphate (UNII: AI9376Y64P) (Dexamethasone - UNII:7S5I7G3JQL) Dexamethasone Phosphate10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Trisodium Citrate Dihydrate (UNII: B22547B95K)  
    Water (UNII: 059QF0KO0R)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Citric Acid Monohydrate (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:25021-053-0125 in 1 CARTON12/01/2024
    11 mL in 1 VIAL; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21565412/01/2024
    Labeler - Sagent Pharmaceuticals (080579617)