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    NDC 68788-6778-09 Sumatriptan 100 mg/1 Details

    Sumatriptan 100 mg/1

    Sumatriptan is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is SUMATRIPTAN SUCCINATE.

    Product Information

    NDC 68788-6778
    Product ID 68788-6778_c441bcc1-c732-40d8-a962-f2b4377a5d16
    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
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sumatriptan Succinate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name SUMATRIPTAN SUCCINATE
    Labeler Name Preferred Pharmaceuticals, Inc.
    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 ANDA078327
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-6778-09 (68788677809)

    NDC Package Code 68788-6778-9
    Billing NDC 68788677809
    Package 1 BLISTER PACK in 1 CARTON (68788-6778-9) / 9 TABLET in 1 BLISTER PACK
    Marketing Start Date 2016-10-24
    NDC Exclude Flag N
    Pricing Information N/A