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Tobrex
Tobrex - 21695-458-35 - (tobramycin)
Drug Information of Tobrex
| Product NDC: | 21695-458 |
| Proprietary Name: | Tobrex |
| Non Proprietary Name: | tobramycin |
| Active Ingredient(s): | 3 mg/g & nbsp; tobramycin |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tobrex
| Product NDC: | 21695-458 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050555 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19811125 |
Package Information of Tobrex
| Package NDC: | 21695-458-35 |
| Package Description: | 3.5 g in 1 TUBE (21695-458-35) |
NDC Information of Tobrex
| NDC Code | 21695-458-35 |
| Proprietary Name | Tobrex |
| Package Description | 3.5 g in 1 TUBE (21695-458-35) |
| Product NDC | 21695-458 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tobramycin |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19811125 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | TOBRAMYCIN |
| Strength Number | 3 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
