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) 012249
Active Ingredient(s): CHLORDIAZEPOXIDE HYDROCHLORIDE
Company: VALEANT PHARM INTL
 
Label History
 
Labels are not available on this site for LIBRIUM, (NDA) 012249
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
6/2/1983 047Manufacturing Change or Addition  
1/26/1982 045Control Supplement  
1/26/1982 044Control Supplement  
6/3/1980 043Labeling Revision  
10/25/1979 042Labeling Revision  
7/24/1978 041Expiration Date Change  
3/31/1978 040Labeling Revision  
2/18/1977 039Formulation Revision  
2/18/1977 038Formulation Revision  
12/14/1976 036Labeling Revision  
10/18/1976 035Labeling Revision  
4/29/1974 026Control Supplement  
2/24/1960 000Approval  
 
Therapeutic Equivalents
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