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    NDC 31722-0678-56 Varenicline 0.5 mg/1 Details

    Varenicline 0.5 mg/1

    Varenicline is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Camber Pharmaceuticals, Inc.. The primary component is VARENICLINE TARTRATE.

    Product Information

    NDC 31722-0678
    Product ID 31722-678_09a2708f-ed1b-b986-e063-6394a90a8fb5
    Associated GPIs
    GCN Sequence Number 060896
    GCN Sequence Number Description varenicline tartrate TABLET 0.5 MG ORAL
    HIC3 J3C
    HIC3 Description SMOKING DETERRENT-NICOTINIC RECEPT.PARTIAL AGONIST
    GCN 27046
    HICL Sequence Number 033766
    HICL Sequence Number Description VARENICLINE TARTRATE
    Brand/Generic Generic
    Proprietary Name Varenicline
    Proprietary Name Suffix n/a
    Non-Proprietary Name Varenicline tartrate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 0.5
    Active Ingredient Units mg/1
    Substance Name VARENICLINE TARTRATE
    Labeler Name Camber Pharmaceuticals, Inc.
    Pharmaceutical Class Cholinergic Agonists [MoA], Cholinergic Receptor Agonist [EPC], Partial Cholinergic Nicotinic Agonist [EPC], Partial Cholinergic Nicotinic Agonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA214571
    Listing Certified Through 2024-12-31

    Package

    NDC 31722-0678-56 (31722067856)

    NDC Package Code 31722-678-56
    Billing NDC 31722067856
    Package 56 TABLET, FILM COATED in 1 BOTTLE (31722-678-56)
    Marketing Start Date 2023-10-23
    NDC Exclude Flag N
    Pricing Information N/A