DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CHLORPROPAMIDE
FDA Application No:
(ANDA) 088852
Active Ingredient(s):
CHLORPROPAMIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for CHLORPROPAMIDE, (ANDA) 088852
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/26/1991
014
Labeling in Effect
11/27/1991
013
Labeling in Effect
1/28/1991
011
Chemistry
5/31/1991
010
Chemistry
6/29/1990
009
Chemistry
6/22/1988
008
Labeling
4/25/1988
007
Chemistry
4/25/1988
006
Chemistry
4/28/1987
004
Chemistry
10/29/1986
002
Chemistry
7/19/1985
001
Chemistry
9/26/1984
000
Approval
Therapeutic Equivalents
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