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    NDC 53329-0643-29 Acetaminophen 650 mg/1 Details

    Acetaminophen 650 mg/1

    Acetaminophen is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Medline Industries, LP. The primary component is ACETAMINOPHEN.

    Product Information

    NDC 53329-0643
    Product ID 53329-643_efd0f6f1-820e-32e8-e053-2a95a90a0e66
    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 Acetaminophen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acetaminophen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 650
    Active Ingredient Units mg/1
    Substance Name ACETAMINOPHEN
    Labeler Name Medline Industries, LP
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076200
    Listing Certified Through 2024-12-31

    Package

    NDC 53329-0643-29 (53329064329)

    NDC Package Code 53329-643-29
    Billing NDC 53329064329
    Package 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53329-643-29)
    Marketing Start Date 2018-07-10
    NDC Exclude Flag N
    Pricing Information N/A