DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PROPRANOLOL HYDROCHLORIDE
FDA Application No:
(ANDA) 070177
Active Ingredient(s):
PROPRANOLOL HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for PROPRANOLOL HYDROCHLORIDE, (ANDA) 070177
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/27/2002
025
Labeling
4/25/2001
024
Control Supplement
10/28/1999
023
Labeling
9/8/1998
021
Labeling
2/18/1993
019
Labeling
6/21/1991
016
Labeling
3/21/1991
015
Labeling in Effect
1/28/1991
013
Chemistry
8/7/1991
012
Chemistry
6/29/1990
011
Chemistry
5/8/1989
011
Labeling
6/29/1988
010
Chemistry
6/29/1988
009
Chemistry
12/22/1988
008
Chemistry
5/8/1989
007
Labeling
3/25/1988
006
Chemistry
12/22/1987
004
Chemistry
5/13/1986
000
Approval
Therapeutic Equivalents
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