DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ASTRAMORPH PF
FDA Application No:
(ANDA) 071050
Active Ingredient(s):
MORPHINE SULFATE
Company:
ABRAXIS BIOSCIENCE
Label History
Labels are not available on this site for ASTRAMORPH PF, (ANDA) 071050
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/2/2002
008
Labeling
12/12/1997
006
Chemistry
7/2/1996
005
Chemistry
12/20/1988
003
Labeling
12/20/1988
002
Chemistry
12/20/1988
001
Chemistry
10/7/1986
000
Approval
Therapeutic Equivalents
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