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    NDC 47682-0037-50 Belmora Flanax 220 mg/1 Details

    Belmora Flanax 220 mg/1

    Belmora Flanax is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Unifirst First Aid Corporation. The primary component is NAPROXEN SODIUM.

    Product Information

    NDC 47682-0037
    Product ID 47682-037_ebf3deb7-0831-d81b-e053-2a95a90ae3be
    Associated GPIs
    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 Belmora Flanax
    Proprietary Name Suffix n/a
    Non-Proprietary Name Naproxen Sodium
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 220
    Active Ingredient Units mg/1
    Substance Name NAPROXEN SODIUM
    Labeler Name Unifirst First Aid Corporation
    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 ANDA079096
    Listing Certified Through 2024-12-31

    Package

    NDC 47682-0037-50 (47682003750)

    NDC Package Code 47682-037-50
    Billing NDC 47682003750
    Package 50 PACKET in 1 BOX (47682-037-50) / 1 TABLET, FILM COATED in 1 PACKET
    Marketing Start Date 2008-12-30
    NDC Exclude Flag N
    Pricing Information N/A
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