Search by Drug Name or NDC

    NDC 68788-9682-03 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 Preferred Pharmaceuticals, Inc.. The primary component is ALPRAZOLAM.

    Product Information

    NDC 68788-9682
    Product ID 68788-9682_28a776a4-65f4-4581-882d-350aa1bd3f41
    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 Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Benzodiazepine [EPC], Benzodiazepines [CS]
    DEA Schedule CIV
    Marketing Category ANDA
    Application Number ANDA090871
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-9682-03 (68788968203)

    NDC Package Code 68788-9682-3
    Billing NDC 68788968203
    Package 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-9682-3)
    Marketing Start Date 2013-04-22
    NDC Exclude Flag N
    Pricing Information N/A