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    NDC 71205-0595-30 Naproxen 220 mg/1 Details

    Naproxen 220 mg/1

    Naproxen is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is NAPROXEN SODIUM.

    Product Information

    NDC 71205-0595
    Product ID 71205-595_0193d608-f4a8-5a69-e063-6294a90aafe8
    Associated GPIs 66100060100303
    GCN Sequence Number 021980
    GCN Sequence Number Description naproxen sodium TABLET 220 MG ORAL
    HIC3 S2B
    HIC3 Description NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS
    GCN 47132
    HICL Sequence Number 003726
    HICL Sequence Number Description NAPROXEN SODIUM
    Brand/Generic Generic
    Proprietary Name Naproxen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Naproxen Sodium
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 220
    Active Ingredient Units mg/1
    Substance Name NAPROXEN SODIUM
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204872
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0595-30 (71205059530)

    NDC Package Code 71205-595-30
    Billing NDC 71205059530
    Package 30 TABLET in 1 BOTTLE (71205-595-30)
    Marketing Start Date 2021-07-27
    NDC Exclude Flag N
    Pricing Information N/A