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    NDC 70518-2995-00 Butalbital, Acetaminophen, Caffeine 325; 50; 40 mg/1; mg/1; mg/1 Details

    Butalbital, Acetaminophen, Caffeine 325; 50; 40 mg/1; mg/1; mg/1

    Butalbital, Acetaminophen, Caffeine is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is ACETAMINOPHEN; BUTALBITAL; CAFFEINE.

    Product Information

    NDC 70518-2995
    Product ID 70518-2995_eb3de85f-ffd7-1e9f-e053-2995a90a8985
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Butalbital, Acetaminophen, Caffeine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Butalbital, Acetaminophen, and Caffeine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 325; 50; 40
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name ACETAMINOPHEN; BUTALBITAL; CAFFEINE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Barbiturate [EPC], Barbiturates [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]
    DEA Schedule CIII
    Marketing Category ANDA
    Application Number ANDA209587
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2995-00 (70518299500)

    NDC Package Code 70518-2995-0
    Billing NDC 70518299500
    Package 30 TABLET, COATED in 1 BLISTER PACK (70518-2995-0)
    Marketing Start Date 2021-01-19
    NDC Exclude Flag N
    Pricing Information N/A