Label: NORGESIC- orphenadrine citrate, aspirin and caffeine tablet, multilayer NORGESIC FORTE- orphenadrine citrate, aspirin and caffeine tablet, multilayer 

  • NDC Code(s): 0089-0231-10, 0089-0231-50, 0089-0233-10, 0089-0233-50
  • Packager: 3M Pharmaceuticals
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status:

Drug Label Information

Updated 05/06

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  • SPL UNCLASSIFIED SECTION

    TABLETS

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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 Norgesic 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

    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. Norgesic and Norgesic Forte do not directly relax tense skeletal muscles in man.

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  • CONTRAINDICATIONS

    Because of the mild anticholinergic effect of orphenadrine, Norgesic or Norgesic Forte should not be used in patients with glaucoma, pyloric or duodenal obstruction, achalasia, prostatic hypertrophy or obstructions at the bladder neck. Norgesic or Norgesic Forte is 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. Norgesic and Norgesic Forte contain aspirin and therefore are not recommended for use in patients with chicken pox, influenza, or flu symptoms.

    Norgesic and Norgesic Forte 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.

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  • USAGE IN PREGNANCY

    Since safety of the use of this preparation in pregnancy, during lactation, or in the childbearing 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.

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  • PEDIATRIC USE

    Safety and effectiveness in pediatric patients have not been established.

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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 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 Norgesic and Norgesic Forte has not been established; therefore, if Norgesic or Norgesic Forte is prescribed for prolonged use, periodic monitoring of blood, urine and liver function values is recommended.

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  • ADVERSE REACTIONS

    Side effects of Norgesic or Norgesic Forte 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, dilatation 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 Norgesic has been reported. No causal relationship has been established. Rare G.I. hemorrhage due to aspirin content may be associated with the administration of Norgesic or Norgesic Forte. Some patients may experience transient episodes of light-headedness, dizziness or syncope.

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  • DOSAGE AND ADMINISTRATION

    Norgesic: Adults 1 to 2 tablets 3 to 4 times daily.

    Norgesic Forte: Adults ½ to 1 tablet 3 to 4 times daily.

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  • HOW SUPPLIED

    Norgesic tablets can be identified by their two layers colored white and yellow. Each round tablet is embossed “NORGESIC” on one side and “3M” on the other and contains orphenadrine citrate (2-dimethylaminoethyl 2-methylbenzhydryl ether citrate) 25 mg, aspirin 385 mg, and caffeine 30 mg.

    Norgesic Forte tablets are exactly twice the strength of Norgesic. They are identified by their scored capsule shape and by their two layers colored white and yellow. Each capsule shaped tablet is embossed “NORGESIC FORTE” on one side and “3M” on the other and contains orphenadrine citrate 50 mg, aspirin 770 mg, and caffeine 60 mg.

    Norgesic and Norgesic Forte also contain: lactose, polyethylene glycol, povidone, starch, sucrose, zinc stearate, and D&C yellow #10.

    Norgesic: Bottles of 100 tablets (NDC 0089-0231-10) and 500 tablets (NDC 0089-0231-50).

    Norgesic Forte: Bottles of 100 tablets (NDC 0089-0233-10) and 500 tablets (NDC 0089-0233-50).

    Store below 30°C (86°F).

    Rx only

    600600 MAY 1998

    3M Pharmaceuticals

    Northridge, CA 91324

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  • INGREDIENTS AND APPEARANCE
    NORGESIC 
    orphenadrine citrate, aspirin and caffeine tablet, multilayer
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0089-0231
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    orphenadrine citrate (orphenadrine) 25 mg
    aspirin (aspirin) 385 mg
    caffeine (caffeine) 30 mg
    Inactive Ingredients
    Ingredient Name Strength
    lactose  
    polyethylene glycol  
    povidone  
    starch  
    sucrose  
    zinc stearate  
    D&C yellow #10  
    Product Characteristics
    Color WHITE (WHITE) Score no score
    Shape ROUND (ROUND ) Size 11mm
    Flavor Imprint Code NORGESIC;3M
    Contains     
    Coating false Symbol false
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0089-0231-10 100 in 1 BOTTLE
    2 NDC:0089-0231-50 500 in 1 BOTTLE
    NORGESIC FORTE 
    orphenadrine citrate, aspirin and caffeine tablet, multilayer
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0089-0233
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    orphenadrine citrate (orphenadrine) 50 mg
    aspirin (aspirin) 770 mg
    caffeine (caffeine) 60 mg
    Inactive Ingredients
    Ingredient Name Strength
    lactose  
    polyethylene glycol  
    povidone  
    starch  
    sucrose  
    zinc stearate  
    D&C yellow #10  
    Product Characteristics
    Color WHITE (WHITE) Score 2 pieces
    Shape OVAL (CAPSULE ) Size 19mm
    Flavor Imprint Code NORGESIC FORTE;3M
    Contains     
    Coating false Symbol false
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0089-0233-10 100 in 1 BOTTLE
    2 NDC:0089-0233-50 500 in 1 BOTTLE
    Labeler - 3M Pharmaceuticals
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