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    NDC 47335-0410-88 Sumatriptan and Naproxen Sodium 500; 85 mg/1; mg/1 Details

    Sumatriptan and Naproxen Sodium 500; 85 mg/1; mg/1

    Sumatriptan and Naproxen Sodium is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE.

    Product Information

    NDC 47335-0410
    Product ID 47335-410_e0e3ea6e-7931-4279-880d-9d4f7d340acf
    Associated GPIs 67992002600320
    GCN Sequence Number 063885
    GCN Sequence Number Description sumatriptan succ/naproxen sod TABLET 85MG-500MG ORAL
    HIC3 H3F
    HIC3 Description ANTIMIGRAINE PREPARATIONS
    GCN 99597
    HICL Sequence Number 035534
    HICL Sequence Number Description SUMATRIPTAN SUCCINATE/NAPROXEN SODIUM
    Brand/Generic Generic
    Proprietary Name Sumatriptan and Naproxen Sodium
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sumatriptan and Naproxen Sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 500; 85
    Active Ingredient Units mg/1; mg/1
    Substance Name NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE
    Labeler Name Sun Pharmaceutical Industries, Inc.
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], 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 ANDA202803
    Listing Certified Through 2024-12-31

    Package

    NDC 47335-0410-88 (47335041088)

    NDC Package Code 47335-410-88
    Billing NDC 47335041088
    Package 100 TABLET, FILM COATED in 1 BOTTLE (47335-410-88)
    Marketing Start Date 2018-07-20
    NDC Exclude Flag N
    Pricing Information N/A