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    NDC 43598-0060-52 Naproxen Sodium 220 mg/1 Details

    Naproxen Sodium 220 mg/1

    Naproxen Sodium is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Dr.Reddy's Laboratories Inc. The primary component is NAPROXEN SODIUM.

    Product Information

    NDC 43598-0060
    Product ID 43598-060_583abf1f-c5f3-baeb-3e5d-9e645247116d
    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 Back and Muscle Pain Caplets
    Non-Proprietary Name Naproxen Sodium
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 220
    Active Ingredient Units mg/1
    Substance Name NAPROXEN SODIUM
    Labeler Name Dr.Reddy's Laboratories Inc
    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 ANDA075168
    Listing Certified Through 2024-12-31

    Package

    NDC 43598-0060-52 (43598006052)

    NDC Package Code 43598-060-52
    Billing NDC 43598006052
    Package 225 TABLET, COATED in 1 BOTTLE (43598-060-52)
    Marketing Start Date 2021-08-05
    NDC Exclude Flag N
    Pricing Information N/A