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    NDC 00173-0735-00 IMITREX 25 mg/1 Details

    IMITREX 25 mg/1

    IMITREX is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by GlaxoSmithKline LLC. The primary component is SUMATRIPTAN SUCCINATE.

    Product Information

    NDC 00173-0735
    Product ID 0173-0735_d11a0873-59af-493c-be1a-9c5adf68182c
    Associated GPIs 67406070100305
    GCN Sequence Number 023799
    GCN Sequence Number Description sumatriptan succinate TABLET 25 MG ORAL
    HIC3 H3F
    HIC3 Description ANTIMIGRAINE PREPARATIONS
    GCN 05702
    HICL Sequence Number 006587
    HICL Sequence Number Description SUMATRIPTAN SUCCINATE
    Brand/Generic Brand
    Proprietary Name IMITREX
    Proprietary Name Suffix n/a
    Non-Proprietary Name sumatriptan
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name SUMATRIPTAN SUCCINATE
    Labeler Name GlaxoSmithKline LLC
    Pharmaceutical Class Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA020132
    Listing Certified Through 2024-12-31

    Package

    NDC 00173-0735-00 (00173073500)

    NDC Package Code 0173-0735-00
    Billing NDC 00173073500
    Package 1 CARTON in 1 CARTON (0173-0735-00) / 1 BLISTER PACK in 1 CARTON / 9 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2003-12-17
    NDC Exclude Flag N
    Pricing Information N/A