Search by Drug Name or NDC

    NDC 68788-7180-01 Glyburide and Metformin Hydrochloride 2.5; 500 mg/1; mg/1 Details

    Glyburide and Metformin Hydrochloride 2.5; 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 Preferred Pharmaceuticals Inc.. The primary component is GLYBURIDE; METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 68788-7180
    Product ID 68788-7180_4f83f783-3e86-4550-a346-a56c079abb5b
    Associated GPIs 27997002400320
    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 2.5; 500
    Active Ingredient Units mg/1; mg/1
    Substance Name GLYBURIDE; METFORMIN HYDROCHLORIDE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS], Sulfonylurea Compounds [CS], Sulfonylurea [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077870
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7180-01 (68788718001)

    NDC Package Code 68788-7180-1
    Billing NDC 68788718001
    Package 100 TABLET, FILM COATED in 1 BOTTLE (68788-7180-1)
    Marketing Start Date 2018-07-16
    NDC Exclude Flag N
    Pricing Information N/A