DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
FAMOTIDINE
FDA Application No:
(ANDA) 075512
Active Ingredient(s):
FAMOTIDINE
Company:
IVAX PHARMS
Label History
Labels are not available on this site for FAMOTIDINE, (ANDA) 075512
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/8/2002
003
Control Supplement
1/17/2002
002
Facility Addition
1/17/2002
001
Facility Addition
7/26/2001
000
Approval
Therapeutic Equivalents
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