Product NDC: | 54868-6083 |
Proprietary Name: | Tamiflu |
Non Proprietary Name: | oseltamivir phosphate |
Active Ingredient(s): | 45 mg/1 & nbsp; oseltamivir phosphate |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-6083 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021087 |
Marketing Category: | NDA |
Start Marketing Date: | 20091030 |
Package NDC: | 54868-6083-0 |
Package Description: | 1 BLISTER PACK in 1 CARTON (54868-6083-0) > 10 CAPSULE in 1 BLISTER PACK |
NDC Code | 54868-6083-0 |
Proprietary Name | Tamiflu |
Package Description | 1 BLISTER PACK in 1 CARTON (54868-6083-0) > 10 CAPSULE in 1 BLISTER PACK |
Product NDC | 54868-6083 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | oseltamivir phosphate |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20091030 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | OSELTAMIVIR PHOSPHATE |
Strength Number | 45 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Neuraminidase Inhibitor [EPC],Neuraminidase Inhibitors [MoA] |