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    NDC 70934-0690-30 GLYBURIDE 2.5 mg/1 Details

    GLYBURIDE 2.5 mg/1

    GLYBURIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is GLYBURIDE.

    Product Information

    NDC 70934-0690
    Product ID 70934-690_d608d942-0e61-4afe-e053-2995a90afdc5
    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 GLYBURIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name GLYBURIDE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 2.5
    Active Ingredient Units mg/1
    Substance Name GLYBURIDE
    Labeler Name Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090937
    Listing Certified Through n/a

    Package

    NDC 70934-0690-30 (70934069030)

    NDC Package Code 70934-690-30
    Billing NDC 70934069030
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70934-690-30)
    Marketing Start Date 2020-04-30
    NDC Exclude Flag N
    Pricing Information N/A
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