RELENZA is a Respiratory (inhalation) Powder in the Human Prescription Drug category. It is labeled and distributed by Dispensing Solutions Inc.. The primary component is Zanamivir.
Product ID | 68258-3030_342b7e19-49d6-4d0b-950a-cc00f4b79924 |
NDC | 68258-3030 |
Product Type | Human Prescription Drug |
Proprietary Name | RELENZA |
Generic Name | Zanamivir |
Dosage Form | Powder |
Route of Administration | RESPIRATORY (INHALATION) |
Marketing Start Date | 2002-12-22 |
Marketing Category | NDA / NDA |
Application Number | NDA021036 |
Labeler Name | Dispensing Solutions Inc. |
Substance Name | ZANAMIVIR |
Active Ingredient Strength | 5 mg/1 |
Pharm Classes | Neuraminidase Inhibitor [EPC],Neuraminidase Inhibitors [MoA] |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2002-12-22 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA021036 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2002-12-22 |
Inactivation Date | 2019-10-21 |
Ingredient | Strength |
---|---|
ZANAMIVIR | 5 mg/1 |
SPL SET ID: | 12ff22f6-20b5-4fa8-9028-58f87e169ff5 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0173-0681 | RELENZA | zanamivir |
68258-3030 | RELENZA | zanamivir |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RELENZA 78452022 3049319 Live/Registered |
Glaxo Group Limited 2004-07-16 |
RELENZA 75975285 2101718 Dead/Cancelled |
Glaxo Group Limited 1994-06-21 |
RELENZA 74540557 not registered Dead/Abandoned |
Glaxo Group Limited 1994-06-21 |