Search by Drug Name or NDC

    NDC 46708-0020-71 MEPROBAMATE 400 mg/1 Details

    MEPROBAMATE 400 mg/1

    MEPROBAMATE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Alembic Pharmaceuticals Limited. The primary component is MEPROBAMATE.

    Product Information

    NDC 46708-0020
    Product ID 46708-020_8c5c7ad8-a128-4243-bd03-0e7057295b3f
    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 MEPROBAMATE
    Proprietary Name Suffix n/a
    Non-Proprietary Name MEPROBAMATE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 400
    Active Ingredient Units mg/1
    Substance Name MEPROBAMATE
    Labeler Name Alembic Pharmaceuticals Limited
    Pharmaceutical Class n/a
    DEA Schedule CIV
    Marketing Category ANDA
    Application Number ANDA090122
    Listing Certified Through 2024-12-31

    Package

    NDC 46708-0020-71 (46708002071)

    NDC Package Code 46708-020-71
    Billing NDC 46708002071
    Package 100 TABLET in 1 BOTTLE (46708-020-71)
    Marketing Start Date 2013-07-23
    NDC Exclude Flag N
    Pricing Information N/A