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Tobramycin and Dexamethasone
Tobramycin and Dexamethasone - 52125-536-01 - (Tobramycin and Dexamethasone)
Drug Information of Tobramycin and Dexamethasone
| Product NDC: | 52125-536 |
| Proprietary Name: | Tobramycin and Dexamethasone |
| Non Proprietary Name: | Tobramycin and Dexamethasone |
| Active Ingredient(s): | 1; 3 mg/mL; mg/mL & nbsp; Tobramycin and Dexamethasone |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SUSPENSION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tobramycin and Dexamethasone
| Product NDC: | 52125-536 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064134 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130603 |
Package Information of Tobramycin and Dexamethasone
| Package NDC: | 52125-536-01 |
| Package Description: | 5 mL in 1 BOTTLE, DROPPER (52125-536-01) |
NDC Information of Tobramycin and Dexamethasone
| NDC Code | 52125-536-01 |
| Proprietary Name | Tobramycin and Dexamethasone |
| Package Description | 5 mL in 1 BOTTLE, DROPPER (52125-536-01) |
| Product NDC | 52125-536 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tobramycin and Dexamethasone |
| Dosage Form Name | SUSPENSION/ DROPS |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20130603 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | DEXAMETHASONE; TOBRAMYCIN |
| Strength Number | 1; 3 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient] |
