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:
(NDA) 019999
Active Ingredient(s):
MORPHINE SULFATE
Company:
MERIDIAN MEDCL TECHN
Label History
Labels are not available on this site for MORPHINE SULFATE, (NDA) 019999
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/29/2002
008
Control Supplement
12/18/2001
007
Control Supplement
11/21/2000
006
Package Change
12/14/1999
005
Manufacturing Change or Addition
7/13/1999
004
Control Supplement
10/23/1998
003
Manufacturing Change or Addition
10/28/1997
002
Control Supplement
3/27/1996
001
Package Change
7/12/1990
000
Approval
There are no Therapeutic Equivalents
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