Search by Drug Name or NDC

    NDC 70010-0131-31 Acetaminophen and Ibuprofen 250; 125 mg/1; mg/1 Details

    Acetaminophen and Ibuprofen 250; 125 mg/1; mg/1

    Acetaminophen and Ibuprofen is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Granules Pharmaceuticals Inc.. The primary component is ACETAMINOPHEN; IBUPROFEN.

    Product Information

    NDC 70010-0131
    Product ID 70010-131_00acf0ce-9a5a-7359-e063-6394a90a9766
    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 and Ibuprofen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acetaminophen and Ibuprofen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 250; 125
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; IBUPROFEN
    Labeler Name Granules 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 ANDA216592
    Listing Certified Through 2024-12-31

    Package

    NDC 70010-0131-31 (70010013131)

    NDC Package Code 70010-131-31
    Billing NDC 70010013131
    Package 288 TABLET in 1 BOTTLE (70010-131-31)
    Marketing Start Date 2023-07-24
    NDC Exclude Flag N
    Pricing Information N/A