| 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] |