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    NDC 49314-0993-03 Unishield Ibuprofen 200 mg/1 Details

    Unishield Ibuprofen 200 mg/1

    Unishield Ibuprofen is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Unishield. The primary component is IBUPROFEN.

    Product Information

    NDC 49314-0993
    Product ID 49314-0993_da470a75-6c2b-13dd-e053-2995a90ad8ee
    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 Unishield Ibuprofen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ibuprofen
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name IBUPROFEN
    Labeler Name Unishield
    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 ANDA075010
    Listing Certified Through 2023-12-31

    Package

    NDC 49314-0993-03 (49314099303)

    NDC Package Code 49314-0993-3
    Billing NDC 49314099303
    Package 50 PACKET in 1 BOX (49314-0993-3) / 2 TABLET, COATED in 1 PACKET
    Marketing Start Date 2021-03-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL b9e2e2ba-e2ad-eace-e053-2995a90aed35 Details

    Revised: 3/2022