DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
SELEGILINE HYDROCHLORIDE
FDA Application No:
(ANDA) 075145
Active Ingredient(s):
SELEGILINE HYDROCHLORIDE
Company:
AAIPHARMA LLC
Original Approval or Tentative Approval Date:
September 15, 2003
There are no Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
SELEGILINE HYDROCHLORIDE
SELEGILINE HYDROCHLORIDE
5MG
CAPSULE; ORAL
Discontinued
No
None
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