DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
AVITA
FDA Application No:
(NDA) 020400
Active Ingredient(s):
TRETINOIN
Company:
MYLAN BERTEK
Label History
Labels are not available on this site for AVITA, (NDA) 020400
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/6/2001
003
Manufacturing Change or Addition
12/15/1999
002
Package Change
1/29/1998
000
Approval
Letter
Review
There are no Therapeutic Equivalents
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