DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NANDROLONE DECANOATE
FDA Application No:
(ANDA) 086385
Active Ingredient(s):
NANDROLONE DECANOATE
Company:
WATSON LABS
Label History
Labels are not available on this site for NANDROLONE DECANOATE, (ANDA) 086385
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/19/1999
028
Microbiology
2/2/1999
027
Microbiology
12/8/1997
026
Chemistry
12/4/1996
025
Microbiology
6/29/1995
024
Chemistry
3/4/1993
023
Labeling in Effect
2/11/1991
022
Labeling in Effect
11/21/1989
021
Labeling in Effect
6/21/1989
017
Labeling
2/1/1989
016
Chemistry
2/1/1989
015
Chemistry
2/1/1989
014
Chemistry
6/8/1988
012
Labeling
5/2/1986
010
Chemistry
6/7/1984
008
Chemistry
3/8/1989
007
SBA
1/13/1984
006
Chemistry
5/17/1983
004
Chemistry
12/30/1983
003
Chemistry
12/30/1983
001
Chemistry
1/13/1984
000
Approval
Therapeutic Equivalents
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