DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PERMETHRIN
FDA Application No:
(ANDA) 074806
Active Ingredient(s):
PERMETHRIN
Company:
ACTAVIS MID ATLANTIC
Label History
Labels are not available on this site for PERMETHRIN, (ANDA) 074806
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/19/2002
014
Labeling
4/10/2002
013
Control Supplement
4/10/2002
012
Control Supplement
9/4/2001
011
Control Supplement
9/4/2001
010
Manufacturing Revision
9/4/2001
009
Facility Addition
1/8/2001
008
Package Change
12/29/2000
007
Control Supplement
1/8/2001
006
Control Supplement
11/30/2000
005
Manufacturing Revision
9/21/2000
004
Labeling
9/21/2000
003
Packaging Addition
6/8/1999
002
Chemistry
9/24/1999
001
Labeling
1/23/1998
000
Approval
Review
Therapeutic Equivalents
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