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    NDC 30142-0177-82 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 30142-0177
    Product ID 30142-177_bdcd86be-0ae3-4bf6-ba20-4b5080197a8d
    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 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 30142-0177-82 (30142017782)

    NDC Package Code 30142-177-82
    Billing NDC 30142017782
    Package 200 TABLET, FILM COATED in 1 BOTTLE (30142-177-82)
    Marketing Start Date 2005-02-08
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 4d4f87aa-5189-4037-9c00-d870de81d4dc Details

    Revised: 11/2022