DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PHENTERMINE HYDROCHLORIDE
FDA Application No:
(ANDA) 085319
Active Ingredient(s):
PHENTERMINE HYDROCHLORIDE
Company:
TG UNITED LABS
Label History
Labels are not available on this site for PHENTERMINE HYDROCHLORIDE, (ANDA) 085319
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/6/2000
036
Facility Addition
6/1/1999
034
Labeling
4/8/1998
033
Labeling
12/19/1997
032
Labeling
10/16/1992
030
Chemistry
5/31/1989
028
Chemistry
6/27/1988
027
Chemistry
6/27/1988
026
Chemistry
1/19/1990
025
Labeling
5/12/1983
022
Chemistry
2/4/1983
021
Chemistry
7/15/1986
020
Chemistry
12/16/1982
019
Chemistry
3/14/1977
000
Approval
Therapeutic Equivalents
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