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    NDC 68788-8130-01 Neomycin and Polymyxin B Sulfates and Hydrocortisone 10; 3.5; 10000 mg/mL; mg/mL; [USP'U]/mL Details

    Neomycin and Polymyxin B Sulfates and Hydrocortisone 10; 3.5; 10000 mg/mL; mg/mL; [USP'U]/mL

    Neomycin and Polymyxin B Sulfates and Hydrocortisone is a AURICULAR (OTIC) SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE.

    Product Information

    NDC 68788-8130
    Product ID 68788-8130_e2814386-5b78-45d8-8dc2-398dc77ccbb3
    Associated GPIs 87991003101807
    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 Neomycin and Polymyxin B Sulfates and Hydrocortisone
    Proprietary Name Suffix n/a
    Non-Proprietary Name neomycin sulfate, polymyxin b sulfate and hydrocortisone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SUSPENSION
    Route AURICULAR (OTIC)
    Active Ingredient Strength 10; 3.5; 10000
    Active Ingredient Units mg/mL; mg/mL; [USP'U]/mL
    Substance Name HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Polymyxin-class Antibacterial [EPC], Polymyxins [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA062488
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8130-01 (68788813001)

    NDC Package Code 68788-8130-1
    Billing NDC 68788813001
    Package 10 mL in 1 BOTTLE, PLASTIC (68788-8130-1)
    Marketing Start Date 2022-02-03
    NDC Exclude Flag N
    Pricing Information N/A