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    NDC 70518-2870-00 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 REMEDYREPACK INC.. The primary component is ALPRAZOLAM.

    Product Information

    NDC 70518-2870
    Product ID 70518-2870_04db3876-a2d6-27aa-e063-6294a90ad49f
    Associated GPIs 57100010007510
    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 REMEDYREPACK INC.
    Pharmaceutical Class Benzodiazepine [EPC], Benzodiazepines [CS]
    DEA Schedule CIV
    Marketing Category ANDA
    Application Number ANDA090871
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2870-00 (70518287000)

    NDC Package Code 70518-2870-0
    Billing NDC 70518287000
    Package 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2870-0)
    Marketing Start Date 2020-09-08
    NDC Exclude Flag N
    Pricing Information N/A