Search by Drug Name or NDC

    NDC 43063-0630-30 Glimepiride 2 mg/1 Details

    Glimepiride 2 mg/1

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

    Product Information

    NDC 43063-0630
    Product ID 43063-630_0647abcf-743f-cbed-e063-6294a90ad272
    Associated GPIs 65100075100310
    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 Glimepiride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Glimepiride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 2
    Active Ingredient Units mg/1
    Substance Name GLIMEPIRIDE
    Labeler Name PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078181
    Listing Certified Through 2024-12-31

    Package

    NDC 43063-0630-30 (43063063030)

    NDC Package Code 43063-630-30
    Billing NDC 43063063030
    Package 30 TABLET in 1 BOTTLE, PLASTIC (43063-630-30)
    Marketing Start Date 2015-10-29
    NDC Exclude Flag N
    Pricing Information N/A