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    NDC 51660-0490-41 Ibuprofen and Pseudoephedrine Hydrochloride 200; 30 mg/1; mg/1 Details

    Ibuprofen and Pseudoephedrine Hydrochloride 200; 30 mg/1; mg/1

    Ibuprofen and Pseudoephedrine Hydrochloride is a ORAL TABLET, SUGAR COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Ohm Laboratories Inc.. The primary component is IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE.

    Product Information

    NDC 51660-0490
    Product ID 51660-490_a2971a78-3eb0-4249-b2ec-040b5adf1b21
    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 and Pseudoephedrine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ibuprofen and Pseudoephedrine Hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, SUGAR COATED
    Route ORAL
    Active Ingredient Strength 200; 30
    Active Ingredient Units mg/1; mg/1
    Substance Name IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
    Labeler Name Ohm Laboratories Inc.
    Pharmaceutical Class Adrenergic alpha-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], alpha-Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA074567
    Listing Certified Through 2024-12-31

    Package

    NDC 51660-0490-41 (51660049041)

    NDC Package Code 51660-490-41
    Billing NDC 51660049041
    Package 40 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-490-41)
    Marketing Start Date 2001-10-13
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL c0692a21-358d-47b9-bbff-cc8f4f3bdb56 Details

    Revised: 9/2020