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    NDC 71205-0213-72 Ibuprofen 100 mg/5mL Details

    Ibuprofen 100 mg/5mL

    Ibuprofen is a ORAL SUSPENSION in the HUMAN OTC DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is IBUPROFEN.

    Product Information

    NDC 71205-0213
    Product ID 71205-213_caf36ae7-7d2e-4058-aa5b-35122c1187ab
    Associated GPIs 66100020001820
    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
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ibuprofen
    Product Type HUMAN OTC DRUG
    Dosage Form SUSPENSION
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/5mL
    Substance Name IBUPROFEN
    Labeler Name Proficient Rx LP
    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 ANDA209207
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0213-72 (71205021372)

    NDC Package Code 71205-213-72
    Billing NDC 71205021372
    Package 1 BOTTLE in 1 CARTON (71205-213-72) / 120 mL in 1 BOTTLE
    Marketing Start Date 2019-01-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL b7565aac-a928-4116-b9af-cf636da4537c Details

    Revised: 7/2022