Friday, October 28, 2016

Orphenadrine Aspirin Caffeine





Dosage Form: tablet, multilayer
Orphenadrine Citrate, Aspirin and Caffeine Tablets

Orphenadrine Aspirin Caffeine Description


Each tablet, for oral administration, contains Orphenadrine Citrate USP, 25 mg or 50 mg, Aspirin USP, 385 mg or 770 mg, Caffeine USP, 30 mg or 60 mg.


Orphenadrine citrate, N, N-Dimethyl-2-[(o-methyl-α-phenylbenzyl)oxy]ethylamine citrate (1:1), is a centrally acting (brain stem) compound. It occurs as a white, practically odorless, crystalline powder, having a bitter taste. Its molecular formula is C18H23NO.C6H8O7 with a molecular weight of 461.51. The structural formula is shown below.



Aspirin, salicylic acid acetate, is a non-opiate analgesic, anti-inflammatory and antipyretic agent. It occurs as a white, crystalline tabular or needle like powder and is odorless or has a faint odor. Its molecular formula is C9H8O4, with a molecular weight of 180.16. The structural formula is shown below.



Caffeine, 1,3,7-trimethylxanthine, is a central nervous system stimulant which occurs as a white powder or white glistening needles. It also has a bitter taste. Its molecular formula is C8H10N4O2, with a molecular weight of 194.19. The structural formula is shown below.



Each tablet contains the following inactive ingredients: colloidal silicon dioxide, corn starch, croscarmellose sodium, FD&C Blue No. 1, FD&C Yellow No. 10, anhydrous lactose, microcrystalline cellulose, povidone, pregelatinized starch, stearic acid, and sodium lauryl sulfate.



Orphenadrine Aspirin Caffeine - Clinical Pharmacology


Orphenadrine citrate is a centrally acting (brain stem) compound which in animals selectively blocks facilitatory functions of the reticular formulation. 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 Orphenadrine Citrate, Aspirin, and Caffeine 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.



Indications and Usage for Orphenadrine Aspirin Caffeine


  1. Symptomatic relief of mild to moderate pain of acute musculoskeletal disorders.

  2. 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. Orphenadrine Citrate, Aspirin, and Caffeine Tablets do not directly relax tense skeletal muscles in man.




Contraindications


Because of the mild anti-cholinergic effect of orphenadrine, Orphenadrine Citrate, Aspirin, and Caffeine Tablets should not be used in patients with glaucoma, pyloric or duodenal obstruction, achalasia, prostatic hypertrophy, or obstructions at the bladder neck. Orphenadrine Citrate, Aspirin, and Caffeine Tablets 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.



Warnings


Reye’s Syndrome may develop in individuals who have chicken pox, influenza, or flu symptoms. Some studies suggest possible association between the development of Reye’s Syndrome and the use of medicines containing salicylate or aspirin. Orphenadrine Citrate, Aspirin, and Caffeine Tablets contain aspirin and therefore are not recommended for use in patients with chicken pox, influenza, or flu symptoms. Orphenadrine Citrate, Aspirin, and Caffeine Tablets 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 extreme caution in the presence of peptic ulcers and coagulation abnormalities.



Usage in Pregnancy


Since safety of the use of this preparation in pregnancy, during lactation, or in the child-bearing age has not been established, use of the drug in such patients requires that the potential benefits of the drug be weighed against its possible hazard to the mother and child.



Usage in Children


The safe and effective use of this drug in children has not been established. Usage of this drug in children under 12 years of age is not recommended.



Precautions


Confusion, anxiety and tremors have been reported in a 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.


Safety of continuous long term therapy with Orphenadrine Citrate, Aspirin, and Caffeine Tablets has not been established; therefore, if Orphenadrine Citrate, Aspirin, and Caffeine Tablets are prescribed for prolonged use, periodic monitoring of blood, urine and liver function values is recommended.



Adverse Reactions


Side effects of Orphenadrine Citrate, Aspirin, and Caffeine Tablets 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 Orphenadrine Citrate, Aspirin, and Caffeine Tablets has been reported. No causal relationship has been established. Rare G.I. hemorrhage due to aspirin content may be associated with the administration of Orphenadrine Citrate, Aspirin, and Caffeine Tablets. Some patients may experience transient episodes of lightheadedness, dizziness or syncope.



Orphenadrine Aspirin Caffeine Dosage and Administration


Orphenadrine Citrate, Aspirin, and Caffeine Tablets, 25 mg/385 mg/30 mg: Adults 1 to 2 tablets 3 to 4 times daily.


Orphenadrine Citrate, Aspirin, and Caffeine Tablets, 50 mg/770 mg/60 mg: Adults 1/2 to 1 tablet 3 to 4 times daily.



How is Orphenadrine Aspirin Caffeine Supplied


Orphenadrine Citrate, Aspirin, and Caffeine Tablets, 25 mg/385 mg/30 mg are round, layered tablets colored white and green, imprinted SZ 477 and are supplied as:


NDC 0185-0713-01 bottles of 100


NDC 0185-0713-05 bottles of 500


NDC 0185-0713-10 bottles of 1000


Orphenadrine Citrate, Aspirin, and Caffeine Tablets, 50 mg/770 mg/60 mg are scored, capsule-shaped, layered tablets colored white and green, imprinted SZ 491 and are supplied as:


NDC 0185-0714-01 bottles of 100


NDC 0185-0714-05 bottles of 500



Storage


Store at 20°-25°C (68°-77° F) (see USP Controlled Room Temperature).


Protect from moisture.



03-2008M


7363


Sandoz Inc.


Princeton, NJ 08540




mg/385 mg/30 mg Label


NDC 0185-0713-01


Orphenadrine


Citrate, Aspirin,


and Caffeine


Tablets


25 mg/385 mg/30 mg


Rx only 100 Tablets


SANDOZ




mg/770 mg/60 mg Label


NDC 0185-0714-01


Orphenadrine


Citrate, Aspirin,


and Caffeine


Tablets


50 mg/770 mg/60 mg


Rx only 100 Tablets


SANDOZ










ORPHENADRINE CITRATE, ASPIRIN AND CAFFEINE 
orphenadrine citrate, aspirin and caffeine  tablet, multilayer










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)0185-0713
Route of AdministrationORALDEA Schedule    














Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ORPHENADRINE CITRATE (ORPHENADRINE)ORPHENADRINE CITRATE25 mg
ASPIRIN (ASPIRIN)ASPIRIN385 mg
CAFFEINE (CAFFEINE)CAFFEINE30 mg
























Inactive Ingredients
Ingredient NameStrength
ANHYDROUS LACTOSE 
CELLULOSE, MICROCRYSTALLINE 
CROSCARMELLOSE SODIUM 
D&C YELLOW NO. 10 
FD&C BLUE NO. 1 
POVIDONE 
SILICON DIOXIDE 
SODIUM LAURYL SULFATE 
STARCH, CORN 
STEARIC ACID 


















Product Characteristics
ColorWHITE, GREENScoreno score
ShapeROUNDSize12mm
FlavorImprint CodeSZ477
Contains      


















Packaging
#NDCPackage DescriptionMultilevel Packaging
10185-0713-101000 TABLET In 1 BOTTLENone
20185-0713-05500 TABLET In 1 BOTTLENone
30185-0713-01100 TABLET In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07465412/31/1996







ORPHENADRINE CITRATE, ASPIRIN AND CAFFEINE 
orphenadrine citrate, aspirin and caffeine  tablet, multilayer










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)0185-0714
Route of AdministrationORALDEA Schedule    














Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ORPHENADRINE CITRATE (ORPHENADRINE)ORPHENADRINE CITRATE50 mg
ASPIRIN (ASPIRIN)ASPIRIN770 mg
CAFFEINE (CAFFEINE)CAFFEINE60 mg
























Inactive Ingredients
Ingredient NameStrength
ANHYDROUS LACTOSE 
CROSCARMELLOSE SODIUM 
FD&C BLUE NO. 1 
D&C YELLOW NO. 10 
CELLULOSE, MICROCRYSTALLINE 
POVIDONE 
SILICON DIOXIDE 
SODIUM LAURYL SULFATE 
STARCH, CORN 
STEARIC ACID 


















Product Characteristics
ColorWHITE, GREENScoreno score
ShapeCAPSULESize2mm
FlavorImprint CodeSZ491
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
10185-0714-05500 TABLET In 1 BOTTLENone
20185-0714-01100 TABLET In 1 BOTTLENone










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07465412/31/1996


Labeler - Eon Labs, Inc. (012656273)
Revised: 10/2011Eon Labs, Inc.

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