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    NDC 68788-7800-01 Naproxen Sodium 550 mg/1 Details

    Naproxen Sodium 550 mg/1

    Naproxen Sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is NAPROXEN SODIUM.

    Product Information

    NDC 68788-7800
    Product ID 68788-7800_d27525a3-7d35-445d-b231-3418b1810c40
    Associated GPIs 66100060100310
    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 PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 550
    Active Ingredient Units mg/1
    Substance Name NAPROXEN SODIUM
    Labeler Name Preferred Pharmaceuticals, 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 ANDA212199
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7800-01 (68788780001)

    NDC Package Code 68788-7800-1
    Billing NDC 68788780001
    Package 100 TABLET in 1 BOTTLE (68788-7800-1)
    Marketing Start Date 2020-10-13
    NDC Exclude Flag N
    Pricing Information N/A