DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
RELENZA
FDA Application No:
(NDA) 021036
Active Ingredient(s):
ZANAMIVIR
Company:
GLAXOSMITHKLINE
Original Approval or Tentative Approval Date:
July 26, 1999
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
There are no Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
RELENZA
ZANAMIVIR
5MG
POWDER; INHALATION
Prescription
Yes
None
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