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) 075718
Active Ingredient(s):
FAMOTIDINE
Company:
DR REDDYS LABS LTD
Label History
Labels are not available on this site for FAMOTIDINE, (ANDA) 075718
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/19/2002
003
Control Supplement
12/13/2001
001
Control Supplement
4/16/2001
000
Approval
Letter
7/27/2000
000
Tentative Approval
Letter
11/29/2000
000
Tentative Approval
Letter
Therapeutic Equivalents
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