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) 075758
Active Ingredient(s):
FAMOTIDINE
Company:
DR REDDYS LABS LTD
Label History
Labels are not available on this site for FAMOTIDINE, (ANDA) 075758
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/13/2002
010
Labeling
4/23/2002
009
Control Supplement
12/6/2001
008
Control Supplement
2/22/2002
006
Expiration Date Change
2/22/2002
005
Labeling
2/22/2002
004
Packaging Addition
1/17/2002
002
Packaging Addition
1/17/2002
001
Expiration Date Change
8/17/2001
000
Approval
Letter
12/13/2000
000
Tentative Approval
Letter
Therapeutic Equivalents
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