DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SUCRALFATE
FDA Application No:
(ANDA) 070848
Active Ingredient(s):
SUCRALFATE
Company:
TEVA
Label History
Labels are not available on this site for SUCRALFATE, (ANDA) 070848
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/23/2002
018
Manufacturing Revision
10/23/2002
017
Control Supplement
10/23/2002
016
Manufacturing Revision
5/15/2002
015
Facility Addition
11/13/2001
014
Facility Addition
11/13/2001
013
Control Supplement
8/30/2001
012
Facility Addition
5/29/2001
010
Supplier Addition
8/24/2000
009
Control Supplement
7/7/2000
008
Facility Addition
3/31/2000
007
Control Supplement
2/16/2000
006
Facility Addition
3/26/1999
005
Chemistry
3/12/1999
004
Chemistry
6/18/1997
003
Chemistry
11/8/1996
002
Chemistry
11/8/1996
001
Chemistry
3/29/1996
000
Approval
Review
Therapeutic Equivalents
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