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TobraDex
TobraDex - 21695-628-35 - (tobramycin and dexamethasone)
Drug Information of TobraDex
| Product NDC: | 21695-628 |
| Proprietary Name: | TobraDex |
| Non Proprietary Name: | tobramycin and dexamethasone |
| Active Ingredient(s): | 1; 3 mg/g; mg/g & nbsp; tobramycin and dexamethasone |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TobraDex
| Product NDC: | 21695-628 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050616 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19880928 |
Package Information of TobraDex
| Package NDC: | 21695-628-35 |
| Package Description: | 3.5 g in 1 TUBE (21695-628-35) |
NDC Information of TobraDex
| NDC Code | 21695-628-35 |
| Proprietary Name | TobraDex |
| Package Description | 3.5 g in 1 TUBE (21695-628-35) |
| Product NDC | 21695-628 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | tobramycin and dexamethasone |
| Dosage Form Name | OINTMENT |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19880928 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | DEXAMETHASONE; TOBRAMYCIN |
| Strength Number | 1; 3 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
