Product NDC: | 54868-6315 |
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) |
Product NDC: | 54868-6315 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021246 |
Marketing Category: | NDA |
Start Marketing Date: | 20111103 |
Package NDC: | 54868-6315-0 |
Package Description: | 1 BOTTLE, GLASS in 1 CARTON (54868-6315-0) > 6 mL in 1 BOTTLE, GLASS |
NDC Code | 54868-6315-0 |
Proprietary Name | Tamiflu |
Package Description | 1 BOTTLE, GLASS in 1 CARTON (54868-6315-0) > 6 mL in 1 BOTTLE, GLASS |
Product NDC | 54868-6315 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Oseltamivir Phosphate |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20111103 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | OSELTAMIVIR PHOSPHATE |
Strength Number | 6 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Neuraminidase Inhibitor [EPC],Neuraminidase Inhibitors [MoA] |