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) 086732
Active Ingredient(s):
PHENTERMINE HYDROCHLORIDE
Company:
TG UNITED LABS
Label History
Labels are not available on this site for PHENTERMINE HYDROCHLORIDE, (ANDA) 086732
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/6/2000
026
Facility Addition
11/3/1998
024
Labeling
8/19/1998
023
Labeling
4/8/1998
021
Labeling
12/19/1997
020
Labeling
10/16/1992
019
Chemistry
7/31/1989
017
Labeling
5/31/1989
016
Chemistry
6/27/1988
015
Chemistry
6/27/1988
014
Chemistry
4/26/1984
012
Chemistry
12/20/1983
010
Chemistry
12/20/1983
009
Chemistry
3/28/1983
006
Chemistry
9/10/1980
000
Approval
Therapeutic Equivalents
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