DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
VANCOMYCIN HYDROCHLORIDE
FDA Application No:
(ANDA) 062663
Active Ingredient(s):
VANCOMYCIN HYDROCHLORIDE
Company:
ABRAXIS PHARM
Label History
Labels are not available on this site for VANCOMYCIN HYDROCHLORIDE, (ANDA) 062663
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/5/2002
037
Facility Addition
12/2/2002
036
Facility Addition
12/2/2002
035
Control Supplement
10/18/2001
032
Facility Addition
12/13/2000
030
Control Supplement
12/13/2000
029
Expiration Date Change
9/11/2000
028
Manufacturing Revision
12/13/2000
027
Manufacturing Revision
12/13/2000
026
Package Change
2/1/2000
024
Control Supplement
10/25/1999
023
Control Supplement
10/18/1999
022
Chemistry
2/11/1998
021
Chemistry
11/28/1997
020
Labeling
11/28/1997
019
Chemistry New Strength
7/5/1996
018
Chemistry
3/12/1996
017
Labeling
4/3/1995
016
Labeling
8/4/1992
015
Labeling
11/30/1994
014
Chemistry
11/30/1994
013
Chemistry in Effect
11/20/1990
010
Labeling
6/7/1991
009
Chemistry
12/23/1991
008
Chemistry
8/11/1988
007
Chemistry
6/3/1988
004
Chemistry
3/17/1987
000
Approval
Therapeutic Equivalents
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