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    NDC 51660-0493-41 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 51660-0493
    Product ID 51660-493_f197efd7-d871-49e6-9984-51628bab7e8d
    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 51660-0493-41 (51660049341)

    NDC Package Code 51660-493-41
    Billing NDC 51660049341
    Package 40 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-493-41)
    Marketing Start Date 2001-10-13
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL cb7fb0d3-adf6-4c14-ac61-103dc869ebf2 Details

    Revised: 9/2020