Visitor Monitoring Drug History: LIBRIUM
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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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 DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
12/28/1998 024Manufacturing Change or Addition  
5/7/2002 023Labeling Revision Letter 
2/3/1994 022Control Supplement  
7/16/1992 021Control Supplement  
8/6/1985 019Manufacturing Change or Addition  
5/29/1985 018Manufacturing Change or Addition  
3/29/1985 017Labeling Revision  
2/3/1983 016Manufacturing Change or Addition  
8/21/1980 014Labeling Revision  
5/28/1980 013Labeling Revision  
10/25/1979 012Labeling Revision  
7/20/1979 011Distributor  
11/6/1978 010Labeling Revision  
12/14/1977 008Distributor  
7/21/1961 000Approval  
 
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