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    NDC 10702-0192-50 Hydrocodone Bitartrate and Acetaminophen 300; 5 mg/1; mg/1 Details

    Hydrocodone Bitartrate and Acetaminophen 300; 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 KVK-Tech, Inc.. The primary component is ACETAMINOPHEN; HYDROCODONE BITARTRATE.

    Product Information

    NDC 10702-0192
    Product ID 10702-192_0b4c1153-bdc7-8313-e063-6294a90a3765
    Associated GPIs 65991702100309
    GCN Sequence Number 060338
    GCN Sequence Number Description hydrocodone/acetaminophen TABLET 5 MG-300MG ORAL
    HIC3 H3U
    HIC3 Description OPIOID ANALGESIC AND NON-SALICYLATE ANALGESICS
    GCN 26470
    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 300; 5
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; HYDROCODONE BITARTRATE
    Labeler Name KVK-Tech, Inc.
    Pharmaceutical Class Opioid Agonist [EPC], Opioid Agonists [MoA]
    DEA Schedule CII
    Marketing Category ANDA
    Application Number ANDA209036
    Listing Certified Through 2024-12-31

    Package

    NDC 10702-0192-50 (10702019250)

    NDC Package Code 10702-192-50
    Billing NDC 10702019250
    Package 500 TABLET in 1 BOTTLE (10702-192-50)
    Marketing Start Date 2017-06-22
    NDC Exclude Flag N
    Pricing Information N/A