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    NDC 00006-5364-09 STEGLATRO 15 mg/1 Details

    STEGLATRO 15 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 00006-5364
    Product ID 0006-5364_14d838b4-511b-4585-aa0f-1d61249b5d04
    Associated GPIs 27700055200340
    GCN Sequence Number 078042
    GCN Sequence Number Description ertugliflozin pidolate TABLET 15 MG ORAL
    HIC3 C4D
    HIC3 Description ANTIHYPERGLYCEMIC-SOD/GLUC COTRANSPORT2(SGLT2) INH
    GCN 44259
    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 15
    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 00006-5364-09 (00006536409)

    NDC Package Code 0006-5364-09
    Billing NDC 00006536409
    Package 2 BOTTLE in 1 CARTON (0006-5364-09) / 7 TABLET, FILM COATED in 1 BOTTLE (0006-5364-08)
    Marketing Start Date 2017-12-19
    NDC Exclude Flag N
    Pricing Information N/A