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    NDC 41163-0079-15 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 SUPERVALU INC. The primary component is NAPROXEN SODIUM.

    Product Information

    NDC 41163-0079
    Product ID 41163-079_94ab3a89-85d0-4985-ad99-43bd7bbf9e48
    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 SUPERVALU 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 2024-12-31

    Package

    NDC 41163-0079-15 (41163007915)

    NDC Package Code 41163-079-15
    Billing NDC 41163007915
    Package 1 BOTTLE, PLASTIC in 1 CARTON (41163-079-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
    Marketing Start Date 2019-01-15
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 1aedc0a1-466a-40c6-bb4c-53b7e8f83aff Details

    Revised: 12/2018