DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
METFORMIN HYDROCHLORIDE
FDA Application No:
(ANDA) 076038
Active Ingredient(s):
METFORMIN HYDROCHLORIDE
Company:
MUTUAL PHARMA
Label History
Labels are not available on this site for METFORMIN HYDROCHLORIDE, (ANDA) 076038
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/16/2007
024
Labeling
8/13/2002
004
Labeling
12/12/2002
003
Control Supplement
12/12/2002
002
Control Supplement
12/12/2002
001
Control Supplement
2/21/2002
000
Approval
Letter
Therapeutic Equivalents
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