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    NDC 00065-0631-36 MAXITROL 1; 3.5; 10000 mg/g; mg/g; [USP'U]/g Details

    MAXITROL 1; 3.5; 10000 mg/g; mg/g; [USP'U]/g

    MAXITROL is a OPHTHALMIC OINTMENT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Alcon Laboratories, Inc.. The primary component is DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE.

    Product Information

    NDC 00065-0631
    Product ID 0065-0631_7cafb7c6-1bf0-42d8-aa07-bc544149b50d
    Associated GPIs 86309903324210
    GCN Sequence Number 048546
    GCN Sequence Number Description neomycin/polymyxin B/dexametha OINT. (G) 3.5-10K-.1 OPHTHALMIC
    HIC3 Q6I
    HIC3 Description EYE ANTIBIOTIC AND GLUCOCORTICOID COMBINATIONS
    GCN 14285
    HICL Sequence Number 003523
    HICL Sequence Number Description NEOMYCIN/POLYMYXIN B SULFATE/DEXAMETHASONE
    Brand/Generic Brand
    Proprietary Name MAXITROL
    Proprietary Name Suffix n/a
    Non-Proprietary Name neomycin sulfate, polymyxin b sulfate and dexamethasone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form OINTMENT
    Route OPHTHALMIC
    Active Ingredient Strength 1; 3.5; 10000
    Active Ingredient Units mg/g; mg/g; [USP'U]/g
    Substance Name DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
    Labeler Name Alcon Laboratories, 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 NDA
    Application Number NDA050065
    Listing Certified Through n/a

    Package

    NDC 00065-0631-36 (00065063136)

    NDC Package Code 0065-0631-36
    Billing NDC 00065063136
    Package 3.5 g in 1 TUBE (0065-0631-36)
    Marketing Start Date 1972-01-17
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL d17cecdb-c7cb-41cc-a11e-00c6ed0dcc11 Details

    Revised: 10/2020