DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
METHIMAZOLE
FDA Application No:
(NDA) 040350
Active Ingredient(s):
METHIMAZOLE
Company:
GENPHARM
Label History
Labels are not available on this site for METHIMAZOLE, (NDA) 040350
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/28/2001
006
Package Change
7/10/2001
005
Control Supplement
6/7/2001
004
Labeling
6/7/2001
003
Packaging Addition
Review
6/7/2001
002
Control Supplement
Review
6/7/2001
001
Chemistry New Strength
Review
3/29/2000
000
Approval
Letter
Review
Therapeutic Equivalents
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