DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NIFEDIPINE
FDA Application No:
(ANDA) 075289
Active Ingredient(s):
NIFEDIPINE
Company:
BIOVAIL
Label History
Labels are not available on this site for NIFEDIPINE, (ANDA) 075289
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/16/2002
005
Supplier Addition
6/4/2002
004
Control Supplement
12/28/2001
003
Control Supplement
7/15/2002
002
Control Supplement
2/6/2001
001
Control Supplement
Letter
9/27/2000
000
Approval
Review
7/24/2000
000
Tentative Approval
Review
Therapeutic Equivalents
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