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    NDC 70934-0570-60 Glyburide and Metformin Hydrochloride 5; 500 mg/1; mg/1 Details

    Glyburide and Metformin Hydrochloride 5; 500 mg/1; mg/1

    Glyburide and Metformin Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. dba Northwind Pharmaceuticals. The primary component is GLYBURIDE; METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 70934-0570
    Product ID 70934-570_d9a67616-5766-5a4d-e053-2995a90a6305
    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 and Metformin Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Glyburide and Metformin Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5; 500
    Active Ingredient Units mg/1; mg/1
    Substance Name GLYBURIDE; METFORMIN HYDROCHLORIDE
    Labeler Name Denton Pharma, Inc. dba Northwind Pharmaceuticals
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS], Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077870
    Listing Certified Through n/a

    Package

    NDC 70934-0570-60 (70934057060)

    NDC Package Code 70934-570-60
    Billing NDC 70934057060
    Package 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-570-60)
    Marketing Start Date 2022-03-07
    NDC Exclude Flag N
    Pricing Information N/A
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