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    NDC 71335-1061-07 Naproxen Sodium 220 mg/1 Details

    Naproxen Sodium 220 mg/1

    Naproxen Sodium is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is NAPROXEN SODIUM.

    Product Information

    NDC 71335-1061
    Product ID 71335-1061_3d57ba5c-3a1d-435a-aa4f-9cc709e1b8cf
    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 Naproxen Sodium
    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 Bryant Ranch Prepack
    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 ANDA074661
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-1061-07 (71335106107)

    NDC Package Code 71335-1061-7
    Billing NDC 71335106107
    Package 100 TABLET, FILM COATED in 1 BOTTLE (71335-1061-7)
    Marketing Start Date 2021-12-28
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 3d57ba5c-3a1d-435a-aa4f-9cc709e1b8cf Details

    Revised: 12/2021