Label: ORPHENADRINE CITRATE ASPIRIN CAFFEINE- orphenadrine citrate, aspirin, caffeine tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 50564-554-01, 50564-554-05, 50564-555-01, 50564-555-05 - Packager: Jerome Stevens Pharmaceuticals, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated April 29, 2021
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ACTIONS:
Orphenadrine citrate is a centrally acting (brain stem) compound which in animals selectively blocks facilitatory functions of the reticular formation. Orphenadrine does not produce myoneural block, nor does it affect crossed extensor reflexes. Orphenadrine prevents nicotine-induced convulsions but not those produced by strychnine.
Chronic administration of the regular formula to dogs and rats has revealed no drug-related toxicity. No blood or urine changes were observed, nor were there any macroscopic or microscopic pathological changes detected. Extensive experience with combinations containing aspirin and caffeine has established them as safe agents. The addition of orphenadrine citrate does not alter the toxicity of aspirin and caffeine.
The mode of therapeutic action of orphenadrine has not been clearly identified, but may be related to its analgesic properties. Orphenadrine citrate also possesses anticholinergic actions.
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INDICATIONS:
- Symptomatic relief of mild to moderate pain of acute musculoskeletal disorders.
- The orphenadrine component is indicated as an adjunct to rest, physical therapy, and other measures for the relief of discomfort associated with acute painful musculoskeletal conditions.
The mode of action of orphenadrine has not been clearly identified, but may be related to its analgesic properties. These products do not directly relax tense skeletal muscles in man.
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CONTRAINDICATIONS:
Because of the mild anticholinergic effect of orphenadrine, these products should not be used in patients with glaucoma, pyloric or duodenal obstruction, achalasia, prostatic hypertrophy or obstructions at the bladder neck. These products are also contraindicated in patients with myasthenia gravis and in patients known to be sensitive to aspirin or caffeine.
The drug is contraindicated in patients who have demonstrated a previous hypersensitivity to the drug.
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WARNINGS:
Reye's syndrome may develop in individuals who have chicken pox, influenza, or flu symptoms.
Some studies suggest a possible association between the development of Reye's Syndrome and the use of medicines containing salicylate or aspirin. These products contain aspirin and therefore are not recommended for use in patients with chicken pox, influenza, or flu symptoms.
These products may impair the ability of the patient to engage in potentially hazardous activities such as operating machinery or driving a motor vehicle; ambulatory patients should therefore be cautioned accordingly.
Aspirin should be used with extra caution in the presence of peptic ulcers and coagulation abnormalities.
Fetal Toxicity
Premature Closure of Fetal Ductus Arteriosus:
Avoid use of NSAIDS, including Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets, in pregnant women at about 30 weeks of gestation and later. NSAIDs including Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets, increase the risk of premature closure of the fetal ductus arteriosus at approximately this gestational age.
Oligohydramnios / Neonatal Renal Impairment:
Use of NSAIDs including Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets, at about 20 weeks of gestation or later in pregnancy may cause fetal renal dysfunction leading to oligohydramnios and, in some cases, neonatal renal impairment. These adverse outcomes are seen, on average, after days to weeks of treatment, although oligohydramnios has been infrequently reported as soon as 48 hours after NSAID initiation.
Oligohydramnios is often, but not always, reversible with treatment discontinuation. Complications of prolonged oligohydramnios may, for example, include limb contractures and delayed lung maturation. In some post marketing cases of impaired neonatal renal function, invasive procedures such as exchange transfusion or dialysis were required.
If NSAID treatment is necessary between about 20 weeks and 30 weeks gestation, limit Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets use to the lowest effective dose and shortest duration possible. Consider ultrasound monitoring of amniotic fluid if Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets treatment extends beyond 48 hours. Discontinue Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets if oligohydramnios occurs and follow up according to clinical practice [see PRECAUTIONS; Pregnancy].
Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS)
Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) has been reported in patients taking NSAIDs such as Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets. Some of these events have been fatal or life-threatening. DRESS typically, although not exclusively, presents with fever, rash, lymphadenopathy, and/or facial swelling. Other clinical manifestations may include hepatitis, nephritis, hematological abnormalities, myocarditis, or myositis. Sometimes symptoms of DRESS may resemble an acute viral infection. Eosinophilia is often present. Because this disorder is variable in its presentation, other organ systems not noted here may be involved. It is important to note that early manifestations of hypersensitivity, such as fever or lymphadenopathy, may be present even though rash is not evident. If such signs or symptoms are present, discontinue Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets and evaluate the patient immediately.
Pregnancy:
Risk Summary
Withdrawal seizures were reported in a two-day-old male infant whose mother had taken a butalbital-containing drug during the last 2 months of pregnancy. Butalbital was found in the infant's serum. The infant was given phenobarbital 5 mg/kg, which was tapered without further seizure or other withdrawal symptoms.
Use of NSAIDs, including aspirin, can cause premature closure of the fetal ductus arteriosus and fetal renal dysfunction leading to oligohydramnios and, in some cases, neonatal renal impairment. Because of these risks, limit dose and duration of Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets use between about 20 and 30 weeks of gestation, and avoid Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets use at about 30 weeks of gestation and later in pregnancy [see WARNINGS; Fetal Toxicity].
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Premature Closure of Fetal Ductus Arteriosus
Use of NSAIDs, including aspirin, at about 30 weeks gestation or later in pregnancy increases the risk of premature closure of the fetal ductus arteriosus.
Oligohydramnios/Neonatal Renal Impairment
Use of NSAIDs at about 20 weeks gestation or later in pregnancy has been associated with cases of fetal renal dysfunction leading to oligohydramnios, and in some cases, neonatal renal impairment.
Data from observational studies regarding other potential embryofetal risks of NSAID use in women in the first or second trimesters of pregnancy are inconclusive.
Based on animal data, prostaglandins have been shown to have an important role in endometrial vascular permeability, blastocyst implantation, and decidualization. In animal studies, administration of prostaglandin synthesis inhibitors such as aspirin, resulted in increased pre- and post-implantation loss. Prostaglandins also have been shown to have an important role in fetal kidney development. In published animal studies, prostaglandin synthesis inhibitors have been reported to impair kidney development when administered at clinically relevant doses.
The estimated background risk of major birth defects and miscarriage for the indicated population(s) 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 2-4% and 15-20%, respectively.
Clinical Considerations
Fetal/Neonatal Adverse Reactions
Premature Closure of Fetal Ductus Arteriosus:
Avoid use of NSAIDs in women at about 30 weeks gestation and later in pregnancy, because NSAIDs, including Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets, can cause premature closure of the fetal ductus arteriosus (see WARNINGS; Fetal Toxicity).
Oligohydramnios/Neonatal Renal Impairment
If an NSAID is necessary at about 20 weeks gestation or later in pregnancy, limit the use to the lowest effective dose and shortest duration possible. If Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets treatment extends beyond 48 hours, consider monitoring with ultrasound for oligohydramnios. If oligohydramnios occurs, discontinue Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets and follow up according to clinical practice (see WARNINGS; Fetal Toxicity).
Data
Human Data
Premature Closure of Fetal Ductus Arteriosus:
Published literature reports that the use of NSAIDs at about 30 weeks of gestation and later in pregnancy may cause premature closure of the fetal ductus arteriosus.
Oligohydramnios/Neonatal Renal Impairment:
Published studies and post marketing reports describe maternal NSAID use at about 20 weeks gestation or later in pregnancy associated with fetal renal dysfunction leading to oligohydramnios, and in some cases, neonatal renal impairment. These adverse outcomes are seen, on average, after days to weeks of treatment, although oligohydramnios has been infrequently reported as soon as 48 hours after NSAID initiation. In many cases, but not all, the decrease in amniotic fluid was transient and reversible with cessation of the drug. There have been a limited number of case reports of maternal NSAID use and neonatal renal dysfunction without oligohydramnios, some of which were irreversible. Some cases of neonatal renal dysfunction required treatment with invasive procedures, such as exchange transfusion or dialysis.
Methodological limitations of these post marketing studies and reports include lack of a control group; limited information regarding dose, duration, and timing of drug exposure; and concomitant use of other medications. These limitations preclude establishing a reliable estimate of the risk of adverse fetal and neonatal outcomes with maternal NSAID use. Because the published safety data on neonatal outcomes involved mostly preterm infants, the generalizability of certain reported risks to the full-term infant exposed to NSAIDs through maternal use is uncertain.
- USAGE IN CHILDREN:
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PRECAUTIONS:
Confusion, anxiety and tremors have been reported in a few patients receiving propoxyphene and orphenadrine concomitantly. As these symptoms may be simple due to an additive effect, reduction of dosage and/or discontinuation of one or both agents is recommended in such cases.
Safety of continuous long-term therapy with these products has not been established; therefore, if they are prescribed for prolonged use, periodic monitoring of blood, urine and liver function values is recommended.
Pregnancy
Embryo-Fetal Toxicity
Inform pregnant women to avoid use of aspirin and other NSAIDs starting at 30 weeks gestation because of the risk of the premature closing of the fetal ductus arteriosus. If treatment with Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets is needed for a pregnant woman between about 20 to 30 weeks gestation, advise her that she may need to be monitored for oligohydramnios, if treatment continues for longer than 48 hours [see WARNINGS; Fetal Toxicity, PRECAUTIONS; Pregnancy].
Serious Skin Reactions, including DRESS
Advise patients to stop taking Orphenadrine Citrate Aspirin Caffeine Regular and Forte Tablets immediately if they develop any type of rash or fever and to contact their healthcare provider as soon as possible [see Warnings].
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ADVERSE REACTIONS:
Side effects of these products are those seen with aspirin and caffeine or those usually associated with mild anticholinergic agents. These may include tachycardia, palpitation, urinary hesitancy or retention, dry mouth, blurred vision, dilation of the pupil, increased intraocular tension, weakness, nausea, vomiting, headache, dizziness, constipation, drowsiness, and rarely, urticaria and other dermatoses. Infrequently, an elderly patient may experience some degree of confusion. Mild central excitation and occasional hallucinations may be observed. These mild side effects can usually be eliminated by reduction in dosage. One case of aplastic anemia associated with the use of the regular formula has been reported. No causal relationship has been established. Rare G.I. hemorrhage due to aspirin content may be associated with the administration of these products. Some patients may experience transient episodes of lightheadedness, dizziness or syncope.
To report SUSPECTED ADVERSE REACTIONS, contact Jerome Stevens Pharmaceuticals Inc. at 1-844-686-1019 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
- DOSAGE AND ADMINISTRATION:
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HOW SUPPLIED:
Regular tablets can be identified as a round, multi-layered tablet embossed JSP 554 on one side, and contains orphenadrine citrate (2-dimethylaminoethyl 2-methylbenzhydryl ether citrate) 25 mg, aspirin 385 mg, and caffeine 30 mg.
Forte tablets are exactly twice the strength of the regular. They are identified by their scored capsule shape. Each multi-layered tablet is embossed JSP 555 on one side and contains orphenadrine citrate 50 mg, aspirin 770 mg, and caffeine 60 mg.
Products also contain: lactose, starch, D&C yellow #10 and FD&C blue #1.
Regular: Bottles of
100 tablets NDC 50564-554-01 500 tablets NDC 50564-554-05 Forte: Bottles of
100 tablets NDC 50564-555-01 500 tablets NDC 50564-555-05 Store below 30°C (86°F)
Caution:
Federal law prohibits dispensing without prescription.
Manufactured by:
Jerome Stevens Pharmaceuticals, Inc.
Bohemia, NY 11716Rev. 03/21
MG # 11584 - Principal Display Panel - 25 mg Bottle Label
- Principal Display Panel - 50 mg Bottle Label
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INGREDIENTS AND APPEARANCE
ORPHENADRINE CITRATE ASPIRIN CAFFEINE
orphenadrine citrate, aspirin, caffeine tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50564-554 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength orphenadrine citrate (UNII: X0A40N8I4S) (orphenadrine - UNII:AL805O9OG9) orphenadrine citrate 25 mg aspirin (UNII: R16CO5Y76E) (aspirin - UNII:R16CO5Y76E) aspirin 385 mg caffeine (UNII: 3G6A5W338E) (caffeine - UNII:3G6A5W338E) caffeine 30 mg Inactive Ingredients Ingredient Name Strength lactose, unspecified form (UNII: J2B2A4N98G) starch, corn (UNII: O8232NY3SJ) d&c yellow no. 10 (UNII: 35SW5USQ3G) fd&c blue no. 1 (UNII: H3R47K3TBD) Product Characteristics Color green (green) , white ( white) , yellow ( yellow) Score no score Shape ROUND (ROUND) Size 11mm Flavor Imprint Code JSP;554 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50564-554-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 04/30/1999 2 NDC:50564-554-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 04/30/1999 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA074988 04/30/1999 ORPHENADRINE CITRATE ASPIRIN CAFFEINE
orphenadrine citrate, aspirin, caffeine tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:50564-555 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength orphenadrine citrate (UNII: X0A40N8I4S) (orphenadrine - UNII:AL805O9OG9) orphenadrine citrate 50 mg aspirin (UNII: R16CO5Y76E) (aspirin - UNII:R16CO5Y76E) aspirin 770 mg caffeine (UNII: 3G6A5W338E) (caffeine - UNII:3G6A5W338E) caffeine 60 mg Inactive Ingredients Ingredient Name Strength lactose, unspecified form (UNII: J2B2A4N98G) starch, corn (UNII: O8232NY3SJ) d&c yellow no. 10 (UNII: 35SW5USQ3G) fd&c blue no. 1 (UNII: H3R47K3TBD) Product Characteristics Color green (green) , white ( white) , yellow ( yellow) Score 2 pieces Shape CAPSULE (CAPSULE) Size 19mm Flavor Imprint Code JSP;555 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50564-555-01 100 in 1 BOTTLE; Type 0: Not a Combination Product 04/30/1999 2 NDC:50564-555-05 500 in 1 BOTTLE; Type 0: Not a Combination Product 04/30/1999 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA074988 04/30/1999 Labeler - Jerome Stevens Pharmaceuticals, Inc. (021130638) Establishment Name Address ID/FEI Business Operations Jerome Stevens Pharmaceuticals, Inc. 021130638 MANUFACTURE(50564-554, 50564-555) , PACK(50564-554, 50564-555)
