DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BENZAMYCIN PAK
FDA Application No:
(NDA) 050769
Active Ingredient(s):
BENZOYL PEROXIDE; ERYTHROMYCIN
Company:
SANOFI AVENTIS US
Label History
Labels are not available on this site for BENZAMYCIN PAK, (NDA) 050769
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/1/2002
008
Manufacturing Change or Addition
8/28/2002
007
Manufacturing Change or Addition
10/23/2002
006
Manufacturing Change or Addition
9/3/2002
005
Manufacturing Change or Addition
10/17/2001
004
Package Change
10/17/2001
003
Control Supplement
6/29/2001
002
Manufacturing Change or Addition
3/22/2001
001
Manufacturing Change or Addition
11/27/2000
000
Approval
Review
There are no Therapeutic Equivalents
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