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    NDC 76420-0651-30 Alprazolam 1 mg/1 Details

    Alprazolam 1 mg/1

    Alprazolam is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Asclemed USA, Inc.. The primary component is ALPRAZOLAM.

    Product Information

    NDC 76420-0651
    Product ID 76420-651_0e42e402-85e4-30a1-e063-6394a90a142c
    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 Alprazolam
    Proprietary Name Suffix n/a
    Non-Proprietary Name Alprazolam
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 1
    Active Ingredient Units mg/1
    Substance Name ALPRAZOLAM
    Labeler Name Asclemed USA, Inc.
    Pharmaceutical Class Benzodiazepine [EPC], Benzodiazepines [CS]
    DEA Schedule CIV
    Marketing Category ANDA
    Application Number ANDA090871
    Listing Certified Through 2025-12-31

    Package

    NDC 76420-0651-30 (76420065130)

    NDC Package Code 76420-651-30
    Billing NDC 76420065130
    Package 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-651-30)
    Marketing Start Date 2024-01-05
    NDC Exclude Flag N
    Pricing Information N/A