DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ZELAPAR
FDA Application No:
(NDA) 021479
Active Ingredient(s):
SELEGILINE HYDROCHLORIDE
Company:
VALEANT PHARM INTL
Original Approval or Tentative Approval Date:
June 14, 2006
Chemical Type:
3 New dosage form
Review Classification:
S Standard 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
ZELAPAR
SELEGILINE HYDROCHLORIDE
1.25MG
TABLET, ORALLY DISINTEGRATING; ORAL
Prescription
Yes
None
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