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TOBREX
TOBREX - 0065-0644-35 - (tobramycin)
Drug Information of TOBREX
| Product NDC: | 0065-0644 |
| 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: | 0065-0644 |
| Labeler Name: | Alcon Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050555 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19810628 |
Package Information of TOBREX
| Package NDC: | 0065-0644-35 |
| Package Description: | 3.5 g in 1 TUBE (0065-0644-35) |
NDC Information of TOBREX
| NDC Code | 0065-0644-35 |
| Proprietary Name | TOBREX |
| Package Description | 3.5 g in 1 TUBE (0065-0644-35) |
| Product NDC | 0065-0644 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tobramycin |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19810628 |
| Marketing Category Name | NDA |
| Labeler Name | Alcon Laboratories, Inc. |
| Substance Name | TOBRAMYCIN |
| Strength Number | 3 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
