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MAXITROL
MAXITROL - 0065-0631-36 - (neomycin sulfate, polymyxin b sulfate and dexamethasone)
Drug Information of MAXITROL
| Product NDC: | 0065-0631 |
| Proprietary Name: | MAXITROL |
| Non Proprietary Name: | neomycin sulfate, polymyxin b sulfate and dexamethasone |
| Active Ingredient(s): | 1; 3.5; 10000 mg/g; mg/g; [USP'U]/g & nbsp; neomycin sulfate, polymyxin b sulfate and dexamethasone |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MAXITROL
| Product NDC: | 0065-0631 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050065 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19720117 |
Package Information of MAXITROL
| Package NDC: | 0065-0631-36 |
| Package Description: | 3.5 g in 1 TUBE (0065-0631-36) |
NDC Information of MAXITROL
| NDC Code | 0065-0631-36 |
| Proprietary Name | MAXITROL |
| Package Description | 3.5 g in 1 TUBE (0065-0631-36) |
| Product NDC | 0065-0631 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | neomycin sulfate, polymyxin b sulfate and dexamethasone |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19720117 |
| Marketing Category Name | NDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE |
| Strength Number | 1; 3.5; 10000 |
| Strength Unit | mg/g; mg/g; [USP'U]/g |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
