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    NDC 64764-0335-60 KAZANO 12.5; 500 mg/1; mg/1 Details

    KAZANO 12.5; 500 mg/1; mg/1

    KAZANO is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Takeda Pharmaceuticals America, Inc.. The primary component is ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 64764-0335
    Product ID 64764-335_7e03a27c-c802-48a0-801c-785f55f1df36
    Associated GPIs 27992502100320
    GCN Sequence Number 070526
    GCN Sequence Number Description alogliptin benz/metformin HCl TABLET 12.5-500MG ORAL
    HIC3 C4F
    HIC3 Description ANTIHYPERGLYCEMIC,DPP-4 INHIBITOR-BIGUANIDE COMBS.
    GCN 34087
    HICL Sequence Number 039970
    HICL Sequence Number Description ALOGLIPTIN BENZOATE/METFORMIN HCL
    Brand/Generic Brand
    Proprietary Name KAZANO
    Proprietary Name Suffix n/a
    Non-Proprietary Name alogliptin and metformin hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 12.5; 500
    Active Ingredient Units mg/1; mg/1
    Substance Name ALOGLIPTIN BENZOATE; METFORMIN HYDROCHLORIDE
    Labeler Name Takeda Pharmaceuticals America, Inc.
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS], Dipeptidyl Peptidase 4 Inhibitor [EPC], Dipeptidyl Peptidase 4 Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA203414
    Listing Certified Through 2024-12-31

    Package

    NDC 64764-0335-60 (64764033560)

    NDC Package Code 64764-335-60
    Billing NDC 64764033560
    Package 60 TABLET, FILM COATED in 1 BOTTLE (64764-335-60)
    Marketing Start Date 2013-01-25
    NDC Exclude Flag N
    Pricing Information N/A