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) 071051
Active Ingredient(s):
MORPHINE SULFATE
Company:
ABRAXIS BIOSCIENCE
Label History
Labels are not available on this site for ASTRAMORPH PF, (ANDA) 071051
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/2/2002
012
Labeling
12/22/1997
010
Chemistry
5/31/1996
009
Chemistry
8/25/1995
008
Chemistry
5/3/1989
007
Labeling
4/19/1988
006
Chemistry
4/19/1988
005
Chemistry
10/7/1986
000
Approval
Therapeutic Equivalents
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