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) 074054
Active Ingredient(s):
NORTRIPTYLINE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for NORTRIPTYLINE HYDROCHLORIDE, (ANDA) 074054
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/8/2002
015
Labeling
11/6/2001
014
Control Supplement
8/3/2001
013
Control Supplement
5/5/1999
011
Chemistry
6/9/1999
010
Chemistry
3/12/1999
009
Chemistry
4/5/1999
008
Labeling
4/5/1999
007
Chemistry
9/29/1997
006
Labeling
12/12/1997
005
Chemistry
7/31/1996
004
Chemistry
4/5/1995
003
Labeling
8/24/1993
002
Labeling in Effect
9/22/1993
001
Chemistry in Effect
12/31/1992
000
Approval
Therapeutic Equivalents
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