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Tobramycin and Dexamethasone
Tobramycin and Dexamethasone - 52959-984-05 - (Tobramycin and Dexamethasone)
Drug Information of Tobramycin and Dexamethasone
| Product NDC: | 52959-984 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tobramycin and Dexamethasone
| Product NDC: | 52959-984 |
| Labeler Name: | H.J. Harkins Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050592 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20090102 |
Package Information of Tobramycin and Dexamethasone
| Package NDC: | 52959-984-05 |
| Package Description: | 5 mL in 1 BOTTLE (52959-984-05) |
NDC Information of Tobramycin and Dexamethasone
| NDC Code | 52959-984-05 |
| Proprietary Name | Tobramycin and Dexamethasone |
| Package Description | 5 mL in 1 BOTTLE (52959-984-05) |
| Product NDC | 52959-984 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Tobramycin and Dexamethasone |
| Dosage Form Name | SUSPENSION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20090102 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | DEXAMETHASONE; TOBRAMYCIN |
| Strength Number | 1; 3 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Aminoglycoside Antibacterial [EPC],Aminoglycosides [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
