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    NDC 30142-0617-71 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 Kroger Company. The primary component is NAPROXEN SODIUM.

    Product Information

    NDC 30142-0617
    Product ID 30142-617_33442fc5-86a9-4fd7-810c-6c93065e1bf1
    Associated GPIs
    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 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 Kroger Company
    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 n/a

    Package

    NDC 30142-0617-71 (30142061771)

    NDC Package Code 30142-617-71
    Billing NDC 30142061771
    Package 1 BOTTLE in 1 CARTON (30142-617-71) / 50 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 1997-01-16
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 02f012e3-8278-4a8b-9cdf-6d14843c8a78 Details

    Revised: 11/2022