DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
MORPHINE SULFATE
FDA Application No:
(ANDA) 075295
Active Ingredient(s):
MORPHINE SULFATE
Company:
ENDO PHARMS
Label History
Labels are not available on this site for MORPHINE SULFATE, (ANDA) 075295
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/6/2002
014
Manufacturing Revision
11/6/2002
013
Control Supplement
11/26/2001
012
Manufacturing Revision
8/15/2001
011
Manufacturing Revision
1/25/2001
010
Control Supplement
9/15/2000
009
Labeling
9/15/2000
008
Chemistry New Strength
9/15/2000
007
Facility Addition
9/15/2000
006
Labeling
9/15/2000
005
Chemistry New Strength
11/3/1999
004
Control Supplement
8/12/1999
003
Chemistry
10/28/1998
000
Approval
Letter
Review
Therapeutic Equivalents
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