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    NDC 23155-0202-01 Acetamiophen 650 mg/1 Details

    Acetamiophen 650 mg/1

    Acetamiophen is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. The primary component is ACETAMINOPHEN.

    Product Information

    NDC 23155-0202
    Product ID 23155-202_e8b62009-b9ec-4303-86b4-e4abdc210a2c
    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 Acetamiophen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acetaminophen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 650
    Active Ingredient Units mg/1
    Substance Name ACETAMINOPHEN
    Labeler Name Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207035
    Listing Certified Through 2024-12-31

    Package

    NDC 23155-0202-01 (23155020201)

    NDC Package Code 23155-202-01
    Billing NDC 23155020201
    Package 1 BOTTLE in 1 CARTON (23155-202-01) / 100 TABLET, EXTENDED RELEASE in 1 BOTTLE
    Marketing Start Date 2018-06-01
    NDC Exclude Flag N
    Pricing Information N/A