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    NDC 72789-0132-90 Acarbose 50 mg/1 Details

    Acarbose 50 mg/1

    Acarbose is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is ACARBOSE.

    Product Information

    NDC 72789-0132
    Product ID 72789-132_0bdcd623-71ec-5ab8-e063-6294a90acbd9
    Associated GPIs 27500010000320
    GCN Sequence Number 020242
    GCN Sequence Number Description acarbose TABLET 50 MG ORAL
    HIC3 C4M
    HIC3 Description ANTIHYPERGLYCEMIC, ALPHA-GLUCOSIDASE INHIBITORS
    GCN 02319
    HICL Sequence Number 008283
    HICL Sequence Number Description ACARBOSE
    Brand/Generic Generic
    Proprietary Name Acarbose
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acarbose
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name ACARBOSE
    Labeler Name PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class alpha Glucosidase Inhibitors [MoA], alpha-Glucosidase Inhibitor [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078470
    Listing Certified Through 2024-12-31

    Package

    NDC 72789-0132-90 (72789013290)

    NDC Package Code 72789-132-90
    Billing NDC 72789013290
    Package 90 TABLET in 1 BOTTLE, PLASTIC (72789-132-90)
    Marketing Start Date 2022-09-16
    NDC Exclude Flag N
    Pricing Information N/A