Label: ASPIRIN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE - aspirin, caffeine and dihydrocodeine bitartrate capsule 

  • NDC Code(s): 57664-419-88
  • Packager: Caraco Pharmaceutical Laboratories, Ltd
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: CIII
  • Marketing Status: New Drug Application Authorized Generic

Drug Label Information

Updated 05/13

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  • BOXED WARNING(What is this?)

    WARNING: DEATH RELATED TO ULTRA-RAPID METABOLISM OF CODEINE TO MORPHINE
    Respiratory depression and death have occurred in children who received codeine following tonsillectomy and/or adenoidectomy and had evidence of being ultra-rapid metabolizers of codeine due to a CYP2D6 polymorphism.

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  • DESCRIPTION

    Each Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP contains 356.4 mg aspirin, 30 mg caffeine, and 16 mg drocode (dihydrocodeine) bitartrate (Warning–may be habitforming).

    The inactive ingredients present are alginic acid, cellulose, D&C Red 28, FD&C Blue 1, gelatin, iron oxides, stearic acid, and titanium dioxide.

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  • CLINICAL PHARMACOLOGY

    Dihydrocodeine is a semisynthetic narcotic analgesic, related to codeine, with multiple actions qualitatively similar to those of codeine; the most prominent of these involve the central nervous system and organs with smooth-muscle components. The principal action of therapeutic value is analgesia.

    Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP also contains the nonnarcotic antipyretic-analgesic, aspirin.

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  • INDICATIONS AND USAGE

    For the relief of moderate to moderately severe pain.

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  • CONTRAINDICATIONS

    Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP is contraindicated for postoperative pain management in children who have undergone tonsillectomy and/or adenoidectomy.

    Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP is contraindicated in patients with hypersensitivity to dihydrocodeine, codeine, or aspirin.

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  • WARNINGS

    Salicylates should be used with extreme caution in the presence of peptic ulcer or coagulation abnormalities.

    Death Related to Ultra-Rapid Metabolism of Codeine to Morphine

    Respiratory depression and death have occurred in children who received codeine in the post-operative period following tonsillectomy and/or adenoidectomy and had evidence of being ultra-rapid metabolizers of codeine (i.e., multiple copies of the gene for cytochrome P450 isoenzyme 2D6 or high morphine concentrations). Deaths have also occurred in nursing infants who were exposed to high levels of morphine in breast milk because their mothers were ultra-rapid metabolizers of codeine.

    Some individuals may be ultra-rapid metabolizers because of a specific CYP2D6 genotype (gene duplications denoted as *1/*1xN or *1/*2xN). The prevalence of this CYP2D6 phenotype varies widely and has been estimated at 0.5 to 1% in Chinese and Japanese, 0.5 to 1% in Hispanics, 1 to 10% in Caucasians, 3% in African Americans, and 16 to 28% in North Africans, Ethiopians, and Arabs. Data are not available for other ethnic groups. These individuals convert dihydrocodeine into its active metabolite, dihydromorphine, more rapidly and completely than other people. This rapid conversion results in higher than expected serum dihydromorphine levels. Even at labeled dosage regimens, individuals who are ultra-rapid metabolizers may have life-threatening or fatal respiratory depression or experience signs of overdose (such as extreme sleepiness, confusion, or shallow breathing).

    Children with obstructive sleep apnea who are treated with codeine for post-tonsillectomy and/or adenoidectomy pain may be particularly sensitive to the respiratory depressant effects of codeine that has been rapidly metabolized to morphine. Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP is contraindicated for post-operative pain management in all pediatric patients undergoing tonsillectomy and/or adenoidectomy [see Contraindications].

    When prescribing dihydrocodeine-containing drugs, healthcare providers should choose the lowest effective dose for the shortest period of time and inform patients and caregivers about these risks and the signs of dihydromorphine overdose.

    Drug Dependence

    Dihydrocodeine can produce drug dependence of the codeine type and therefore has the potential of being abused. Psychic dependence, physical dependence, and tolerance may develop upon repeated administration of dihydrocodeine, and it should be prescribed and administered with the same degree of caution appropriate to the use of other oral narcotic-containing medications. Like other narcotic-containing medications, dihydrocodeine is subject to the provisions of the Federal Controlled Substances Act.

    Usage in Ambulatory Patients

    Dihydrocodeine may impair the mental and/or physical abilities required for the performance of potentially hazardous tasks, such as driving a car or operating machinery. The patient using Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP should be cautioned accordingly.

    Interactions with other Central Nervous System Depressants

    Patients receiving other narcotic analgesics, general anesthetics, tranquilizers, sedative-hypnotics, or other CNS depressants (including alcohol) concomitantly with Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP may exhibit an additive CNS depression. When such combined therapy is contemplated, the dose of one or both agents should be reduced.

    Usage in Pregnancy

    Reproduction studies have not been performed in animals. There is no adequate information on whether this drug may affect fertility in human males and females or has a teratogenic potential or other adverse effect on the fetus.

    Usage in Nursing Mothers

    Dihydrocodeine bitartrate is secreted into human milk. In women with normal dihydrocodeine metabolism (normal CYP2D6 activity), the amount of dihydrocodeine secreted into human milk is low and dosedependent. However, some women are ultra-rapid metabolizers of dihydrocodeine. These women achieve higher-than-expected serum levels of dihydrocodeine’s active metabolite, dihydromorphine, leading to higher-than-expected levels of dihydromorphine in breast milk and potentially dangerously high serum dihydromorphine levels in their breastfed infants. Therefore, maternal use of dihydrocodeine can potentially lead to serious adverse reactions, including death, in nursing infants.

    The risk of infant exposure to dihydrocodeine and dihydromorphine through breast milk should be weighed against the benefits of breastfeeding for both the mother and the baby. Caution should be exercised when dihydrocodeine is administered to a nursing woman. If a dihydrocodeine containing product is selected, the lowest dose should be prescribed for the shortest period of time to achieve the desired clinical effect. Mothers using dihydrocodeine should be informed about when to seek immediate medical care and how to identify the signs and symptoms of neonatal toxicity, such as drowsiness or sedation, difficulty breastfeeding, breathing difficulties, and decreased tone, in their baby. Nursing mothers who are ultra-rapid metabolizers may also experience overdose symptoms such as extreme sleepiness, confusion, or shallow breathing. Prescribers should closely monitor mother-infant pairs and notify treating pediatricians about the use of dihydrocodeine during breast-feeding [see Warnings].

    Aspirin and caffeine are also excreted in breast milk in small amounts. Because of the potential for serious adverse reactions in nursing infants from this combination product, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

    Usage in Children

    Preparations containing aspirin should be kept out of the reach of children. Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP is not recommended for patients 12 years of age and under. Since there is no experience in chil­dren who have received this drug, safety and efficacy in children have not been established.

    Respiratory depression and death have occurred in children with obstructive sleep apnea who received codeine in the post-operative period following tonsillectomy and/or adenoidectomy and had evidence of being ultra-rapid metabolizers of codeine (i.e., multiple copies of the gene for cytochrome P450 isoenzyme 2D6 or high morphine concentrations). These children may be particularly sensitive to the respiratory depressant effects of codeine that has been rapidly metabolized to morphine. Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP is contraindicated for post-operative pain management in all pediatric patients undergoing tonsillectomy and/or adenoidectomy [see Contraindications].

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  • PRECAUTIONS

    Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP should be given with caution to certain patients, such as the elderly or debilitated.

    Information for Patients

    Advise patients that some people have a genetic variation that results in dihydrocodeine changing into dihydromorphine more rapidly and completely than other people. Most people are unaware of whether they are an ultra-rapid dihydrocodeine metabolizer or not. These higher-than-normal levels of dihydromorphine in the blood may lead to life-threatening or fatal respiratory depression or signs of overdose such as extreme sleepiness, confusion, or shallow breathing. Children with this genetic variation who were prescribed codeine after tonsillectomy and/or adenoidectomy for obstructive sleep apnea may be at greatest risk based on reports of several deaths in this population due to respiratory depression. Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP is contraindicated in all children who undergo tonsillectomy and/or adenoidectomy. Advise caregivers of children receiving Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP for other reasons to monitor for signs of respiratory depression.

    Advise patients that nursing mothers taking dihydrocodeine can have higher dihydromorphine levels in their breast milk if they are ultra-rapid metabolizers. These higher levels of dihydromorphine in breast milk may lead to life-threatening or fatal side effects in nursing babies. Advise nursing mothers to watch for signs of dihydromorphine toxicity in their infants which includes increased sleepiness (more than usual), difficulty breastfeeding, breathing difficulties, or limpness. Instruct nursing mothers to talk to the baby’s doctor immediately if they notice these signs and, if they cannot reach the doctor right away, to take the baby to an emergency room or call 911 (or local emergency services).

    Drug Interactions

    The CNS-depressant effects of Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP may be additive with that of other CNS depressants. See “WARNINGS.”

    Aspirin may enhance the effects of anticoagulants and inhibit the uricosuric effects of uricosuric agents.

    Geriatric Use

    Clinical studies of Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP did not include sufficient numbers of subjects aged 65 and over to determine whether elderly subjects respond differently from younger subjects.

    In general, dose selection for an elderly patient should be cautious, starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy.

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  • ADVERSE REACTIONS

    The most frequently observed reactions include lightheadedness, dizziness, drowsiness, sedation, nausea, vomiting, constipation, pruritus, and skin reactions.

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  • DOSAGE AND ADMINISTRATION

    Dosage should be adjusted according to the severity of the pain and the response of the patient. Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP is given orally. The usual adult dose is two capsules every 4 hours as needed for pain.

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  • HOW SUPPLIED

    Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsule, USP are blue and gray, marked “CP” and “419”, supplied in:

    Bottles of 100 capsules; NDC 57664-419-88

    Store at room temperature, approx. 25°C (77°F).

    Keep tightly closed.

    Dispense in tight container.

                                                       

    carco

    Manufactured by:                                                                                                        C.S. No.:8004T03

    Mikart, Inc.                                                                                                                  Rev. 02/13

    Atlanta, Georgia 30318                                                                                              Code 990C00

    Distributed by:

    Caraco Pharmaceutical Laboratories, Ltd.

    1150 Elijah McCoy Drive

    Detroit, MI 48202

    www.caraco.com

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  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    NDC 57664-419-88

    100 Capsules

    CIII

    Aspirin, Caffeine, and Dihydrocodeine Bitartrate Capsules, USP

    Each capsule contains: 356.4 mg aspirin, 30 mg caffeine and 16 mg drocode (dihydrocodeine) bitartrate (Warning–may be habit-forming).

    SEALED FOR YOUR PROTECTION

    Rx Only

    Caraco Pharmaceutical Laboratories, Ltd.

    Principal Display Panel Text for Carton Label
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  • INGREDIENTS AND APPEARANCE
    ASPIRIN, CAFFEINE, AND DIHYDROCODEINE BITARTRATE 
    aspirin, caffeine, and dihydrocodeine bitartrate capsule
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:57664-419
    Route of Administration ORAL DEA Schedule CIII    
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ASPIRIN (ASPIRIN) ASPIRIN 356.4 mg
    CAFFEINE (CAFFEINE) CAFFEINE 30 mg
    DIHYDROCODEINE BITARTRATE ( DIHYDROCODEINE ) DIHYDROCODEINE BITARTRATE 16 mg
    Inactive Ingredients
    Ingredient Name Strength
    ALGINIC ACID  
    CELLULOSE, MICROCRYSTALLINE  
    D&C RED NO. 28  
    FD&C BLUE NO. 1  
    GELATIN  
    FERROSOFERRIC OXIDE  
    STEARIC ACID  
    TITANIUM DIOXIDE  
    Product Characteristics
    Color BLUE, GRAY Score no score
    Shape CAPSULE Size 19mm
    Flavor Imprint Code CP;419
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:57664-419-88 100 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA AUTHORIZED GENERIC NDA011483 10/01/2012
    Labeler - Caraco Pharmaceutical Laboratories, Ltd (146974886)
    Establishment
    Name Address ID/FEI Business Operations
    Mikart, Inc 030034847 MANUFACTURE(57664-419), PACK(57664-419), ANALYSIS(57664-419)
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