DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MAPROTILINE HYDROCHLORIDE
FDA Application No:
(ANDA) 072163
Active Ingredient(s):
MAPROTILINE HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for MAPROTILINE HYDROCHLORIDE, (ANDA) 072163
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/7/2002
007
Facility Addition
11/10/1999
006
Package Change
8/26/1998
005
Labeling
6/4/1992
004
Labeling in Effect
5/20/1992
003
Labeling
11/29/1990
002
Labeling in Effect
6/1/1988
000
Approval
Therapeutic Equivalents
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