Product NDC: | 68258-3030 |
Proprietary Name: | RELENZA |
Non Proprietary Name: | zanamivir |
Active Ingredient(s): | 5 mg/1 & nbsp; zanamivir |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68258-3030 |
Labeler Name: | Dispensing Solutions Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021036 |
Marketing Category: | NDA |
Start Marketing Date: | 20021222 |
Package NDC: | 68258-3030-1 |
Package Description: | 5 PACKAGE in 1 CARTON (68258-3030-1) > 4 POWDER in 1 PACKAGE |
NDC Code | 68258-3030-1 |
Proprietary Name | RELENZA |
Package Description | 5 PACKAGE in 1 CARTON (68258-3030-1) > 4 POWDER in 1 PACKAGE |
Product NDC | 68258-3030 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | zanamivir |
Dosage Form Name | POWDER |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20021222 |
Marketing Category Name | NDA |
Labeler Name | Dispensing Solutions Inc. |
Substance Name | ZANAMIVIR |
Strength Number | 5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Neuraminidase Inhibitor [EPC],Neuraminidase Inhibitors [MoA] |