DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NORTRIPTYLINE HYDROCHLORIDE
FDA Application No:
(ANDA) 074234
Active Ingredient(s):
NORTRIPTYLINE HYDROCHLORIDE
Company:
MYLAN
Label History
Labels are not available on this site for NORTRIPTYLINE HYDROCHLORIDE, (ANDA) 074234
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/23/2002
010
Labeling
7/24/2002
009
Package Change
3/12/1999
008
Chemistry
3/12/1999
007
Chemistry
4/20/1998
006
Labeling
4/20/1998
005
Chemistry
2/5/1998
004
Chemistry
4/20/1998
003
Chemistry
2/18/1997
002
Labeling
6/28/1995
001
Labeling
7/26/1993
000
Approval
Therapeutic Equivalents
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