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    NDC 00009-0068-07 Xanax 3 mg/1 Details

    Xanax 3 mg/1

    Xanax is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PHARMACIA & UPJOHN COMPANY LLC. The primary component is ALPRAZOLAM.

    Product Information

    NDC 00009-0068
    Product ID 0009-0068_07e7906e-b82b-4a85-9f41-b014864a6931
    Associated GPIs 57100010007530
    GCN Sequence Number 052143
    GCN Sequence Number Description alprazolam TAB ER 24H 3 MG ORAL
    HIC3 H20
    HIC3 Description ANTI-ANXIETY - BENZODIAZEPINES
    GCN 19681
    HICL Sequence Number 001617
    HICL Sequence Number Description ALPRAZOLAM
    Brand/Generic Brand
    Proprietary Name Xanax
    Proprietary Name Suffix XR
    Non-Proprietary Name alprazolam
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 3
    Active Ingredient Units mg/1
    Substance Name ALPRAZOLAM
    Labeler Name PHARMACIA & UPJOHN COMPANY LLC
    Pharmaceutical Class Benzodiazepine [EPC], Benzodiazepines [CS]
    DEA Schedule CIV
    Marketing Category NDA
    Application Number NDA021434
    Listing Certified Through 2024-12-31

    Package

    NDC 00009-0068-07 (00009006807)

    NDC Package Code 0009-0068-07
    Billing NDC 00009006807
    Package 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (0009-0068-07)
    Marketing Start Date 2003-01-17
    NDC Exclude Flag N
    Pricing Information N/A