Visitor Monitoring Drug Details: LIBRIUM
 
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Drug Details

Drug Name: LIBRIUM
FDA Application No: (NDA) 012301
Active Ingredient(s): CHLORDIAZEPOXIDE HYDROCHLORIDE
Company: VALEANT PHARM INTL
Original Approval or Tentative Approval Date: July 21, 1961
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
LIBRIUM CHLORDIAZEPOXIDE HYDROCHLORIDE100MG/AMPINJECTABLE; INJECTION Discontinued No None


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