Visitor Monitoring Drug Details: NEFAZODONE HYDROCHLORIDE
 
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Drug Details

Drug Name: NEFAZODONE HYDROCHLORIDE
FDA Application No: (ANDA) 076196
Active Ingredient(s): NEFAZODONE HYDROCHLORIDE
Company: ROXANE
Original Approval or Tentative Approval Date: September 16, 2003
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
NEFAZODONE HYDROCHLORIDE NEFAZODONE HYDROCHLORIDE50MGTABLET; ORAL Discontinued No None
NEFAZODONE HYDROCHLORIDE NEFAZODONE HYDROCHLORIDE100MGTABLET; ORAL Discontinued No None
NEFAZODONE HYDROCHLORIDE NEFAZODONE HYDROCHLORIDE150MGTABLET; ORAL Discontinued No None
NEFAZODONE HYDROCHLORIDE NEFAZODONE HYDROCHLORIDE200MGTABLET; ORAL Discontinued No None
NEFAZODONE HYDROCHLORIDE NEFAZODONE HYDROCHLORIDE250MGTABLET; ORAL Discontinued No None


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