Visitor Monitoring Drug Details: SERZONE
 
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Drug Details

Drug Name: SERZONE
FDA Application No: (NDA) 020152
Active Ingredient(s): NEFAZODONE HYDROCHLORIDE
Company: BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date: December 22, 1994
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
SERZONE NEFAZODONE HYDROCHLORIDE50MGTABLET; ORAL Discontinued No None
SERZONE NEFAZODONE HYDROCHLORIDE100MGTABLET; ORAL Discontinued No None
SERZONE NEFAZODONE HYDROCHLORIDE150MGTABLET; ORAL Discontinued No None
SERZONE NEFAZODONE HYDROCHLORIDE200MGTABLET; ORAL Discontinued No None
SERZONE NEFAZODONE HYDROCHLORIDE250MGTABLET; ORAL Discontinued No None
SERZONE NEFAZODONE HYDROCHLORIDE300MGTABLET; ORAL Discontinued No None


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