DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CHLORHEXIDINE GLUCONATE
FDA Application No:
(ANDA) 074291
Active Ingredient(s):
CHLORHEXIDINE GLUCONATE
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for CHLORHEXIDINE GLUCONATE, (ANDA) 074291
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/23/2000
005
Package Change
10/6/1998
003
Chemistry
12/18/1997
002
Labeling
12/28/1995
000
Approval
Therapeutic Equivalents
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