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) 071791
Active Ingredient(s):
PROPRANOLOL HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for PROPRANOLOL HYDROCHLORIDE, (ANDA) 071791
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/31/2001
013
Control Supplement
11/10/1999
012
Package Change
11/17/1999
011
Labeling
2/9/1999
010
Labeling
6/4/1992
009
Labeling in Effect
2/4/1991
008
Labeling in Effect
9/10/1990
004
Labeling
7/24/1990
003
Labeling
2/28/1990
002
Labeling
7/15/1987
000
Approval
Therapeutic Equivalents
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