DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
AFEDITAB CR
FDA Application No:
(ANDA) 075659
Active Ingredient(s):
NIFEDIPINE
Company:
WATSON LABS
Label History
Labels are not available on this site for AFEDITAB CR, (ANDA) 075659
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/18/2002
004
Packager Addition
3/15/2002
003
Packager Addition
4/5/2002
001
Control Supplement
10/26/2001
000
Approval
Letter
3/20/2001
000
Tentative Approval
Letter
Therapeutic Equivalents
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