DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
GLIPIZIDE
FDA Application No:
(ANDA) 074223
Active Ingredient(s):
GLIPIZIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for GLIPIZIDE, (ANDA) 074223
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/13/2002
008
Control Supplement
6/17/2002
007
Facility Addition
9/25/2001
006
Labeling
9/5/2001
005
Control Supplement
1/20/2000
004
Labeling
11/5/1999
003
Manufacturing Revision
11/10/1999
002
Package Change
7/13/2000
001
Chemistry
2/27/1995
000
Approval
Therapeutic Equivalents
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