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Tamiflu
Tamiflu - 0004-0820-09 - (Oseltamivir Phosphate)
Drug Information of Tamiflu
| Product NDC: | 0004-0820 |
| Proprietary Name: | Tamiflu |
| Non Proprietary Name: | Oseltamivir Phosphate |
| Active Ingredient(s): | 6 mg/mL & nbsp; Oseltamivir Phosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tamiflu
| Product NDC: | 0004-0820 |
| Labeler Name: | Genentech, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021246 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110711 |
Package Information of Tamiflu
| Package NDC: | 0004-0820-09 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (0004-0820-09) > 60 mL in 1 BOTTLE, GLASS |
NDC Information of Tamiflu
| NDC Code | 0004-0820-09 |
| Proprietary Name | Tamiflu |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (0004-0820-09) > 60 mL in 1 BOTTLE, GLASS |
| Product NDC | 0004-0820 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oseltamivir Phosphate |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20110711 |
| Marketing Category Name | NDA |
| Labeler Name | Genentech, Inc. |
| Substance Name | OSELTAMIVIR PHOSPHATE |
| Strength Number | 6 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Neuraminidase Inhibitor [EPC],Neuraminidase Inhibitors [MoA] |
