DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TRETINOIN
FDA Application No:
(ANDA) 075529
Active Ingredient(s):
TRETINOIN
Company:
SPEAR PHARMS
Label History
Labels are not available on this site for TRETINOIN, (ANDA) 075529
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/11/2002
004
Control Supplement
8/13/2001
003
Control Supplement
2/26/2001
002
Control Supplement
2/22/2000
000
Approval
Letter
Review
Therapeutic Equivalents
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