DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CAVERJECT
FDA Application No:
(NDA) 020755
Active Ingredient(s):
ALPROSTADIL
Company:
PFIZER
Label History
Labels are not available on this site for CAVERJECT, (NDA) 020755
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/2/2003
005
Labeling Revision
Letter
12/20/2001
004
Labeling Revision
10/31/1997
000
Approval
Review
There are no Therapeutic Equivalents
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