DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
RANITIDINE
FDA Application No:
(ANDA) 075439
Active Ingredient(s):
RANITIDINE HYDROCHLORIDE
Company:
RANBAXY
Label History
Labels are not available on this site for RANITIDINE, (ANDA) 075439
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/3/2002
007
Control Supplement
10/1/2002
006
Package Change
4/4/2001
005
Control Supplement
11/9/2000
004
Facility Addition
11/9/2000
003
Facility Addition
11/9/2000
002
Facility Addition
4/19/2000
000
Approval
Letter
Therapeutic Equivalents
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