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    NDC 71205-0274-09 sumatriptan succinate 50 mg/1 Details

    sumatriptan succinate 50 mg/1

    sumatriptan succinate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is SUMATRIPTAN SUCCINATE.

    Product Information

    NDC 71205-0274
    Product ID 71205-274_f215f243-2090-4bb5-8499-321d23b96659
    Associated GPIs 67406070100320
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name sumatriptan succinate
    Proprietary Name Suffix n/a
    Non-Proprietary Name sumatriptan succinate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name SUMATRIPTAN SUCCINATE
    Labeler Name Proficient Rx LP
    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 ANDA
    Application Number ANDA078295
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0274-09 (71205027409)

    NDC Package Code 71205-274-09
    Billing NDC 71205027409
    Package 9 BLISTER PACK in 1 CARTON (71205-274-09) / 1 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2019-05-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 9f4d487a-c5f7-4707-976b-64e738c98d45 Details

    Revised: 4/2022