DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NABUMETONE
FDA Application No:
(ANDA) 075590
Active Ingredient(s):
NABUMETONE
Company:
SANDOZ
Label History
Labels are not available on this site for NABUMETONE, (ANDA) 075590
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/9/2002
005
Manufacturing Revision
9/9/2002
004
Package Change
9/9/2002
003
Packager Addition
11/8/2002
002
Control Supplement
11/8/2002
001
Supplier Addition
2/25/2002
000
Approval
Letter
3/21/2001
000
Tentative Approval
Letter
Therapeutic Equivalents
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