Search by Drug Name or NDC

    NDC 71335-0283-02 Zolpidem Tartrate 10 mg/1 Details

    Zolpidem Tartrate 10 mg/1

    Zolpidem Tartrate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is ZOLPIDEM TARTRATE.

    Product Information

    NDC 71335-0283
    Product ID 71335-0283_e35ee2be-2d89-4d87-80e5-4f59378acc0a
    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 Zolpidem Tartrate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Zolpidem Tartrate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name ZOLPIDEM TARTRATE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Central Nervous System Depression [PE], GABA A Agonists [MoA], Pyridines [CS], gamma-Aminobutyric Acid-ergic Agonist [EPC]
    DEA Schedule CIV
    Marketing Category ANDA
    Application Number ANDA076410
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-0283-02 (71335028302)

    NDC Package Code 71335-0283-2
    Billing NDC 71335028302
    Package 60 TABLET, FILM COATED in 1 BOTTLE (71335-0283-2)
    Marketing Start Date 2021-12-27
    NDC Exclude Flag N
    Pricing Information N/A