Home
>
National Drug Code (NDC)
>
Maxitrol
Maxitrol - 0998-0630-06 - (neomycin sulfate, polymyxin b sulfate and dexamethasone)
Drug Information of Maxitrol
| Product NDC: | 0998-0630 |
| Proprietary Name: | Maxitrol |
| Non Proprietary Name: | neomycin sulfate, polymyxin b sulfate and dexamethasone |
| Active Ingredient(s): | 1; 3.5; 10000 mg/mL; mg/mL; [USP'U]/mL & nbsp; neomycin sulfate, polymyxin b sulfate and dexamethasone |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Maxitrol
| Product NDC: | 0998-0630 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050023 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19641115 |
Package Information of Maxitrol
| Package NDC: | 0998-0630-06 |
| Package Description: | 5 mL in 1 BOTTLE, PLASTIC (0998-0630-06) |
NDC Information of Maxitrol
| NDC Code | 0998-0630-06 |
| Proprietary Name | Maxitrol |
| Package Description | 5 mL in 1 BOTTLE, PLASTIC (0998-0630-06) |
| Product NDC | 0998-0630 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | neomycin sulfate, polymyxin b sulfate and dexamethasone |
| Dosage Form Name | SUSPENSION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19641115 |
| 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/mL; mg/mL; [USP'U]/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
