Search by Drug Name or NDC

    NDC 00006-5363-10 STEGLATRO 5 mg/1 Details

    STEGLATRO 5 mg/1

    STEGLATRO is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Merck Sharp & Dohme LLC. The primary component is ERTUGLIFLOZIN PIDOLATE.

    Product Information

    NDC 00006-5363
    Product ID 0006-5363_14d838b4-511b-4585-aa0f-1d61249b5d04
    Associated GPIs 27700055200320
    GCN Sequence Number 078041
    GCN Sequence Number Description ertugliflozin pidolate TABLET 5 MG ORAL
    HIC3 C4D
    HIC3 Description ANTIHYPERGLYCEMIC-SOD/GLUC COTRANSPORT2(SGLT2) INH
    GCN 44248
    HICL Sequence Number 044709
    HICL Sequence Number Description ERTUGLIFLOZIN PIDOLATE
    Brand/Generic Brand
    Proprietary Name STEGLATRO
    Proprietary Name Suffix n/a
    Non-Proprietary Name ertugliflozin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name ERTUGLIFLOZIN PIDOLATE
    Labeler Name Merck Sharp & Dohme LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA209803
    Listing Certified Through 2024-12-31

    Package

    NDC 00006-5363-10 (00006536310)

    NDC Package Code 0006-5363-10
    Billing NDC 00006536310
    Package 30 TABLET, FILM COATED in 1 BOTTLE (0006-5363-10)
    Marketing Start Date 2017-12-19
    NDC Exclude Flag N
    Pricing Information N/A