Search by Drug Name or NDC

    NDC 68788-6769-09 Sumatriptan 25 mg/1 Details

    Sumatriptan 25 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 68788-6769
    Product ID 68788-6769_093e62aa-1e37-43ba-bf38-2ac87ac0337b
    Associated GPIs 67406070100305
    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 25
    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 68788-6769-09 (68788676909)

    NDC Package Code 68788-6769-9
    Billing NDC 68788676909
    Package 9 TABLET in 1 BLISTER PACK (68788-6769-9)
    Marketing Start Date 2016-10-24
    NDC Exclude Flag N
    Pricing Information N/A