DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CAPITROL
FDA Application No:
(NDA) 017594
Active Ingredient(s):
CHLOROXINE
Company:
WESTWOOD SQUIBB
Label History
Labels are not available on this site for CAPITROL, (NDA) 017594
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/8/1989
018
Formulation Revision
8/8/1988
015
Manufacturing Change or Addition
9/15/1987
014
Control Supplement
5/13/1986
013
Control Supplement
2/13/1986
012
Package Change
10/14/1982
010
Control Supplement
3/24/1982
009
Control Supplement
11/13/1984
008
Practioner Draft Labeling
1/30/1981
007
Formulation Revision
6/11/1981
006
Manufacturing Change or Addition
8/14/1980
005
Control Supplement
5/1/1980
004
Control Supplement
1/30/1981
003
Expiration Date Change
4/3/1979
002
Package Change
4/27/1978
001
Labeling Revision
10/19/1976
000
Approval
There are no Therapeutic Equivalents
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