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    NDC 70518-0908-01 Glipizide and Metformin Hydrochloride 5; 500 mg/1; mg/1 Details

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

    Glipizide and Metformin Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is GLIPIZIDE; METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 70518-0908
    Product ID 70518-0908_0a2067a7-6cbb-1084-e063-6394a90a6fec
    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 Glipizide and Metformin Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Glipizide 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 GLIPIZIDE; METFORMIN HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS], Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078905
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-0908-01 (70518090801)

    NDC Package Code 70518-0908-1
    Billing NDC 70518090801
    Package 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0908-1)
    Marketing Start Date 2017-12-27
    NDC Exclude Flag N
    Pricing Information N/A