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:
(NDA) 016419
Active Ingredient(s):
PROPRANOLOL HYDROCHLORIDE
Company:
BAXTER HLTHCARE CORP
Label History
Labels are not available on this site for PROPRANOLOL HYDROCHLORIDE, (NDA) 016419
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/24/2006
026
Labeling Revision
Letter
12/7/2001
025
Manufacturing Change or Addition
2/6/2002
024
Labeling Revision
2/14/2001
023
Manufacturing Change or Addition
8/22/1999
022
Labeling Revision
11/7/1997
021
Labeling Revision
2/14/1990
020
Labeling Revision
12/6/1988
019
Control Supplement
8/12/1988
018
Package Change
6/18/1985
017
Control Supplement
6/23/1982
016
Control Supplement
6/23/1982
015
Control Supplement
3/12/1981
014
Control Supplement
12/12/1978
013
Labeling Revision
1/17/1979
012
Labeling Revision
11/13/1967
000
Approval
Therapeutic Equivalents
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