Search by Drug Name or NDC

    NDC 00597-0385-88 Trijardy XR 12.5; 2.5; 1000 mg/1; mg/1; mg/1 Details

    Trijardy XR 12.5; 2.5; 1000 mg/1; mg/1; mg/1

    Trijardy XR is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Boehringer Ingelheim Pharmaceuticals, Inc.. The primary component is EMPAGLIFLOZIN; LINAGLIPTIN; METFORMIN HYDROCHLORIDE.

    Product Information

    NDC 00597-0385
    Product ID 0597-0385_0cc7f716-30ec-497c-9aa0-4bfbf8b88d3e
    Associated GPIs 27996703407530
    GCN Sequence Number 080711
    GCN Sequence Number Description empaglifloz/linaglip/metformin TAB BP 24H 12.5-2.5MG ORAL
    HIC3 C4Y
    HIC3 Description ANTIHYPERGLY-SGLT-2 INHIB,DPP-4 INHIB,BIGUANIDE CB
    GCN 47671
    HICL Sequence Number 046321
    HICL Sequence Number Description EMPAGLIFLOZIN/LINAGLIPTIN/METFORMIN HCL
    Brand/Generic Brand
    Proprietary Name Trijardy XR
    Proprietary Name Suffix n/a
    Non-Proprietary Name empagliflozin, linagliptin, metformin hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 12.5; 2.5; 1000
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name EMPAGLIFLOZIN; LINAGLIPTIN; METFORMIN HYDROCHLORIDE
    Labeler Name Boehringer Ingelheim Pharmaceuticals, Inc.
    Pharmaceutical Class Biguanide [EPC], Biguanides [CS], Dipeptidyl Peptidase 4 Inhibitor [EPC], Dipeptidyl Peptidase 4 Inhibitors [MoA], Sodium-Glucose Cotransporter 2 Inhibitor [EPC], Sodium-Glucose Transporter 2 Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA212614
    Listing Certified Through 2024-12-31

    Package

    NDC 00597-0385-88 (00597038588)

    NDC Package Code 0597-0385-88
    Billing NDC 00597038588
    Package 1 BOTTLE in 1 CARTON (0597-0385-88) / 14 TABLET, EXTENDED RELEASE in 1 BOTTLE
    Marketing Start Date 2020-04-23
    NDC Exclude Flag N
    Pricing Information N/A