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) 075294
Active Ingredient(s):
RANITIDINE HYDROCHLORIDE
Company:
DR REDDYS LABS LTD
Label History
Labels are not available on this site for RANITIDINE, (ANDA) 075294
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/21/2002
012
Labeling
3/9/2001
011
Control Supplement
3/9/2001
010
Expiration Date Change
3/9/2001
009
Labeling
3/9/2001
008
Packaging Addition
3/16/2001
007
Expiration Date Change
3/16/2001
006
Labeling
11/15/2000
005
Expiration Date Change
11/15/2000
004
Packaging Addition
3/16/2001
003
Package Change
8/10/2000
002
Control Supplement
8/10/2000
001
Control Supplement
3/28/2000
000
Approval
Letter
Letter
1/29/1999
000
Tentative Approval
Letter
Letter
Therapeutic Equivalents
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