| NDC Code | 0078-0771-01 |
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| Package Description | 3.5 g in 1 TUBE (0078-0771-01) |
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| Product NDC | 0078-0771 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Maxitrol |
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| Non-Proprietary Name | Neomycin Sulfate, Polymyxin B Sulfate And Dexamethasone |
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| Dosage Form | OINTMENT |
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| Usage | OPHTHALMIC |
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| Start Marketing Date | 19720117 |
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| End Marketing Date | 20270228 |
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| Marketing Category Name | NDA |
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| Application Number | NDA050065 |
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| Manufacturer | Novartis Pharmaceuticals Corporation |
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| Substance Name | DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
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| Strength | 1; 3.5; 10000 |
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| Strength Unit | mg/g; mg/g; [USP'U]/g |
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| Pharmacy Classes | Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Polymyxin-class Antibacterial [EPC], Polymyxins [CS] |
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