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    NDC 43386-0357-03 Hydrocodone Bitartrate and Acetaminophen 325; 7.5 mg/1; mg/1 Details

    Hydrocodone Bitartrate and Acetaminophen 325; 7.5 mg/1; mg/1

    Hydrocodone Bitartrate and Acetaminophen is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals,Inc.. The primary component is ACETAMINOPHEN; HYDROCODONE BITARTRATE.

    Product Information

    NDC 43386-0357
    Product ID 43386-357_689e6dcd-1bea-4400-ae49-47589f86f983
    Associated GPIs 65991702100358
    GCN Sequence Number 047431
    GCN Sequence Number Description hydrocodone/acetaminophen TABLET 7.5-325 MG ORAL
    HIC3 H3U
    HIC3 Description OPIOID ANALGESIC AND NON-SALICYLATE ANALGESICS
    GCN 12488
    HICL Sequence Number 001730
    HICL Sequence Number Description HYDROCODONE BITARTRATE/ACETAMINOPHEN
    Brand/Generic Generic
    Proprietary Name Hydrocodone Bitartrate and Acetaminophen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Hydrocodone Bitartrate and Acetaminophen
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 325; 7.5
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
    Labeler Name Lupin Pharmaceuticals,Inc.
    Pharmaceutical Class Opioid Agonist [EPC], Opioid Agonists [MoA]
    DEA Schedule CII
    Marketing Category ANDA
    Application Number ANDA206245
    Listing Certified Through 2024-12-31

    Package

    NDC 43386-0357-03 (43386035703)

    NDC Package Code 43386-357-03
    Billing NDC 43386035703
    Package 30 TABLET in 1 BOTTLE (43386-357-03)
    Marketing Start Date 2016-12-01
    NDC Exclude Flag N
    Pricing Information N/A