Label: ORPHENADRINE CITRATE tablet, extended release
63629-1564-3, view more63629-1564-4, 63629-1564-5, 63629-1564-6, 63629-1564-7, 63629-1564-8, 63629-1564-9
- Packager: Bryant Ranch Prepack
- This is a repackaged label.
- Source NDC Code(s): 43386-480
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Updated October 12, 2020
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Orphenadrine citrate is the citrate salt of orphenadrine. It occurs as a white, crystalline powder having a bitter taste. It is practically odorless; sparingly soluble in water, slightly soluble in alcohol. The chemical name of orphenadrine citrate is (±)-N,N-Dimethyl-2-[(o-methyl-α-phenylbenzyl)oxy]ethylamine citrate (1:1) having molecular formula C18H23NO•C6H8O7 and molecular weight of 461.51. It has the following structural formula:
Each tablet for oral administration contains 100 mg orphenadrine citrate. Each Orphenadrine citrate extended- release tablet contains the following inactive ingredients: hydroxypropyl methylcellulose, lactose monohydrate and magnesium stearate.
- CLINICAL PHARMACOLOGY
- INDICATIONS AND USAGE
Orphenadrine citrate extended-release tablets are contraindicated in patients with glaucoma, pyloric or duodenal obstruction, stenosing peptic ulcers, prostatic hypertrophy or obstruction of the bladder neck, cardio-spasm (mega-esophagus) and myasthenia gravis. Orphenadrine citrate tablets are contraindicated in patients who have demonstrated a previous hypersensitivity to the drug.
Some patients may experience transient episodes of light-headedness, dizziness or syncope. Orphenadrine 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.
Confusion, anxiety and tremors have been reported in few patients receiving propoxyphene and orphenadrine concomitantly. As these symptoms may be simply due to an additive effect, reduction of dosage and/or discontinuation of one or both agents is recommended in such cases. Orphenadrine citrate should be used with caution in patients with tachycardia, cardiac decompensation, coronary insufficiency, cardiac arrhythmias.
Safety of continuous long-term therapy with orphenadrine has not been established. Therefore, if orphenadrine is prescribed for prolonged use, periodic monitoring of blood, urine and liver function values is recommended.
Pregnancy Category C
Animal reproduction studies have not been conducted with orphenadrine. It is also not known whether orphenadrine can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Orphenadrine should be given to a pregnant woman only if clearly needed.
Adverse reactions of orphenadrine are mainly due to the mild anticholinergic action of orphenadrine, and are usually associated with higher dosage. Dryness of the mouth is usually the first adverse effect to appear. When the daily dose is increased, possible adverse effects include: tachycardia, palpitation, urinary hesitancy or retention, blurred vision, dilatation of pupils, increased ocular tension, weakness, nausea, vomiting, headache, dizziness, constipation, drowsiness, hypersensitivity reactions, pruritus, hallucinations, agitation, tremor, gastric irritation, and rarely urticaria and other dermatoses. Infrequently, an elderly patient may experience some degree of mental confusion.
These adverse reactions can usually be eliminated by reduction in dosage. Very rare cases of aplastic anemia associated with the use of orphenadrine tablets have been reported. No causal relationship has been established.
- DRUG ABUSE AND DEPENDENCE
Orphenadrine is toxic when overdosed and typically induces anticholinergic effects. In a review of orphenadrine toxicity, the minimum lethal dose was found to be 2 to 3 grams for adults; however, the range of toxicity is variable and unpredictable.
Treatment for orphenadrine overdose is evacuation of stomach contents (when necessary), charcoal at repeated doses, intensive monitoring, and appropriate supportive treatment of any emergent anticholinergic effects.
- DOSAGE AND ADMINISTRATION
NDC: 63629-1564-0 56 TABLET, EXTENDED RELEASE in a BOTTLE
NDC: 63629-1564-8 14 TABLET, EXTENDED RELEASE in a BOTTLE
NDC: 63629-1564-1 20 TABLET, EXTENDED RELEASE in a BOTTLE
NDC: 63629-1564-6 28 TABLET, EXTENDED RELEASE in a BOTTLE
NDC: 63629-1564-5 30 TABLET, EXTENDED RELEASE in a BOTTLE
NDC: 63629-1564-7 45 TABLET, EXTENDED RELEASE in a BOTTLE
NDC: 63629-1564-2 60 TABLET, EXTENDED RELEASE in a BOTTLE
NDC: 63629-1564-4 90 TABLET, EXTENDED RELEASE in a BOTTLE
NDC: 63629-1564-3 100 TABLET, EXTENDED RELEASE in a BOTTLE
NDC: 63629-1564-9 120 TABLET, EXTENDED RELEASE in a BOTTLE
- Orphenadrine Citrate 100mg ER Tablet
INGREDIENTS AND APPEARANCE
orphenadrine citrate tablet, extended release
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63629-1564(NDC:43386-480) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ORPHENADRINE CITRATE (UNII: X0A40N8I4S) (ORPHENADRINE - UNII:AL805O9OG9) ORPHENADRINE CITRATE 100 mg Inactive Ingredients Ingredient Name Strength HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color WHITE Score no score Shape ROUND Size 10mm Flavor Imprint Code NL4 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63629-1564-0 56 in 1 BOTTLE; Type 0: Not a Combination Product 09/22/2006 2 NDC:63629-1564-8 14 in 1 BOTTLE; Type 0: Not a Combination Product 09/22/2006 3 NDC:63629-1564-1 20 in 1 BOTTLE; Type 0: Not a Combination Product 09/22/2006 4 NDC:63629-1564-6 28 in 1 BOTTLE; Type 0: Not a Combination Product 09/22/2006 5 NDC:63629-1564-5 30 in 1 BOTTLE; Type 0: Not a Combination Product 09/22/2006 6 NDC:63629-1564-7 45 in 1 BOTTLE; Type 0: Not a Combination Product 09/22/2006 7 NDC:63629-1564-2 60 in 1 BOTTLE; Type 0: Not a Combination Product 09/22/2006 8 NDC:63629-1564-4 90 in 1 BOTTLE; Type 0: Not a Combination Product 09/22/2006 9 NDC:63629-1564-3 100 in 1 BOTTLE; Type 0: Not a Combination Product 09/22/2006 10 NDC:63629-1564-9 120 in 1 BOTTLE; Type 0: Not a Combination Product 09/22/2006 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA040284 06/19/1998 Labeler - Bryant Ranch Prepack (171714327) Establishment Name Address ID/FEI Business Operations Bryant Ranch Prepack 171714327 REPACK(63629-1564) , RELABEL(63629-1564)