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    NDC 41250-0073-40 Naproxen Sodium 220 mg/1 Details

    Naproxen Sodium 220 mg/1

    Naproxen Sodium is a ORAL CAPSULE, LIQUID FILLED in the HUMAN OTC DRUG category. It is labeled and distributed by MEIJER, INC.. The primary component is NAPROXEN SODIUM.

    Product Information

    NDC 41250-0073
    Product ID 41250-073_1ab1e8f9-e364-4220-b1f7-8a531d931b1b
    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 CAPSULE, LIQUID FILLED
    Route ORAL
    Active Ingredient Strength 220
    Active Ingredient Units mg/1
    Substance Name NAPROXEN SODIUM
    Labeler Name MEIJER, INC.
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021920
    Listing Certified Through n/a

    Package

    NDC 41250-0073-40 (41250007340)

    NDC Package Code 41250-073-40
    Billing NDC 41250007340
    Package 1 BOTTLE, PLASTIC in 1 BOX (41250-073-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
    Marketing Start Date 2014-09-30
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 61af286c-d2b3-4262-9eaa-c971a2659dcb Details

    Revised: 10/2021