Search by Drug Name or NDC

    NDC 11822-0050-01 ibuprofen pm 38; 200 mg/1; mg/1 Details

    ibuprofen pm 38; 200 mg/1; mg/1

    ibuprofen pm is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Rite Aid Corporation. The primary component is DIPHENHYDRAMINE CITRATE; IBUPROFEN.

    Product Information

    NDC 11822-0050
    Product ID 11822-0050_5f945338-3fd2-4b4d-87e2-2405830dd5f6
    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 ibuprofen pm
    Proprietary Name Suffix n/a
    Non-Proprietary Name Diphenhydramine Citrate, Ibuprofen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 38; 200
    Active Ingredient Units mg/1; mg/1
    Substance Name DIPHENHYDRAMINE CITRATE; IBUPROFEN
    Labeler Name Rite Aid Corporation
    Pharmaceutical Class Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA079113
    Listing Certified Through 2024-12-31

    Package

    NDC 11822-0050-01 (11822005001)

    NDC Package Code 11822-0050-1
    Billing NDC 11822005001
    Package 1 BOTTLE in 1 CARTON (11822-0050-1) / 80 TABLET, FILM COATED in 1 BOTTLE
    Marketing Start Date 2009-06-24
    NDC Exclude Flag N
    Pricing Information N/A