DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ELDEPRYL
FDA Application No:
(NDA) 020647
Active Ingredient(s):
SELEGILINE HYDROCHLORIDE
Company:
SOMERSET
Label History
Labels are not available on this site for ELDEPRYL, (NDA) 020647
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/15/2001
004
Control Supplement
8/6/1997
003
Labeling Revision
Review
5/15/1996
000
Approval
Therapeutic Equivalents
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