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    NDC 49483-0699-42 Acetaminophen 650 mg/1 Details

    Acetaminophen 650 mg/1

    Acetaminophen is a ORAL TABLET, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by TIME CAP LABORATORIES, INC.. The primary component is ACETAMINOPHEN.

    Product Information

    NDC 49483-0699
    Product ID 49483-699_eb0bcd1a-2f6b-5e5e-e053-2995a90ab995
    Associated GPIs 64200010000420
    GCN Sequence Number 022123
    GCN Sequence Number Description acetaminophen TABLET ER 650 MG ORAL
    HIC3 H3E
    HIC3 Description ANALGESIC/ANTIPYRETICS,NON-SALICYLATE
    GCN 16910
    HICL Sequence Number 001866
    HICL Sequence Number Description ACETAMINOPHEN
    Brand/Generic Generic
    Proprietary Name Acetaminophen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acetaminophen tablet extended release
    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 TIME CAP LABORATORIES, INC.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA215486
    Listing Certified Through 2024-12-31

    Package

    NDC 49483-0699-42 (49483069942)

    NDC Package Code 49483-699-42
    Billing NDC 49483069942
    Package 1 BOTTLE in 1 CARTON (49483-699-42) / 24 TABLET, EXTENDED RELEASE in 1 BOTTLE
    Marketing Start Date 2022-11-07
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL cd4d0ad4-7206-94c8-e053-2a95a90aaa14 Details

    Revised: 10/2022