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    NDC 42291-0921-90 Pioglitazone Hydrochloride and Metformin Hydrochloride 850; 15 mg/1; mg/1 Details

    Pioglitazone Hydrochloride and Metformin Hydrochloride 850; 15 mg/1; mg/1

    Pioglitazone Hydrochloride and Metformin Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by AvKARE. The primary component is METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE.

    Product Information

    NDC 42291-0921
    Product ID 42291-921_f6cd8e3d-8b02-18e5-e053-6294a90a075f
    Associated GPIs
    GCN Sequence Number 059686
    GCN Sequence Number Description pioglitazone HCl/metformin HCl TABLET 15MG-850MG ORAL
    HIC3 C4T
    HIC3 Description ANTIHYPERGLYCEMIC, THIAZOLIDINEDIONE AND BIGUANIDE
    GCN 25445
    HICL Sequence Number 033202
    HICL Sequence Number Description PIOGLITAZONE HCL/METFORMIN HCL
    Brand/Generic Generic
    Proprietary Name Pioglitazone Hydrochloride and Metformin Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Pioglitazone Hydrochloride and Metformin Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 850; 15
    Active Ingredient Units mg/1; mg/1
    Substance Name METFORMIN HYDROCHLORIDE; PIOGLITAZONE HYDROCHLORIDE
    Labeler Name AvKARE
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS], PPAR alpha [CS], PPAR gamma [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor Activity [MoA], Thiazolidinedione [E
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA200823
    Listing Certified Through 2024-12-31

    Package

    NDC 42291-0921-90 (42291092190)

    NDC Package Code 42291-921-90
    Billing NDC 42291092190
    Package 90 TABLET, FILM COATED in 1 BOTTLE (42291-921-90)
    Marketing Start Date 2023-03-13
    NDC Exclude Flag N
    Pricing Information N/A