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    NDC 11673-0909-75 up and up naproxen sodium 220 mg/1 Details

    up and up naproxen sodium 220 mg/1

    up and up naproxen sodium is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Target Corporation. The primary component is NAPROXEN SODIUM.

    Product Information

    NDC 11673-0909
    Product ID 11673-909_2b57c682-87bc-430e-bacd-dfeabed565cb
    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 up and up 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 Target Corporation
    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 2024-12-31

    Package

    NDC 11673-0909-75 (11673090975)

    NDC Package Code 11673-909-75
    Billing NDC 11673090975
    Package 90 TABLET, FILM COATED in 1 BOTTLE (11673-909-75)
    Marketing Start Date 2022-02-10
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL b0e98603-94e9-474a-88a0-22042f461271 Details

    Revised: 2/2022