DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
AMINOSYN-PF 7%
FDA Application No:
(NDA) 019398
Active Ingredient(s):
AMINO ACIDS
Company:
HOSPIRA
Label History
Labels are not available on this site for AMINOSYNPF 7, (NDA) 019398
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/25/2002
016
Manufacturing Change or Addition
Letter
9/11/2002
015
Control Supplement
6/8/1999
014
Control Supplement
5/5/1997
013
Control Supplement
8/27/1996
012
Control Supplement
7/11/1994
011
Manufacturing Change or Addition
12/30/1993
010
Control Supplement
9/28/1992
009
Manufacturing Change or Addition
8/18/1992
008
Manufacturing Change or Addition
2/10/1992
007
Manufacturing Change or Addition
8/17/1987
006
Labeling Revision
12/15/1986
005
Labeling Revision
12/15/1986
004
Formulation Revision
1/31/1986
001
Control Supplement
9/6/1985
000
Approval
Therapeutic Equivalents
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