DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
LIBRIUM
FDA Application No:
(NDA) 012301
Active Ingredient(s):
CHLORDIAZEPOXIDE HYDROCHLORIDE
Company:
VALEANT PHARM INTL
Label History
Labels are not available on this site for LIBRIUM, (NDA) 012301
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/28/1998
024
Manufacturing Change or Addition
5/7/2002
023
Labeling Revision
Letter
2/3/1994
022
Control Supplement
7/16/1992
021
Control Supplement
8/6/1985
019
Manufacturing Change or Addition
5/29/1985
018
Manufacturing Change or Addition
3/29/1985
017
Labeling Revision
2/3/1983
016
Manufacturing Change or Addition
8/21/1980
014
Labeling Revision
5/28/1980
013
Labeling Revision
10/25/1979
012
Labeling Revision
7/20/1979
011
Distributor
11/6/1978
010
Labeling Revision
12/14/1977
008
Distributor
7/21/1961
000
Approval
There are no Therapeutic Equivalents
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