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FDA ANDA · ANDA076409

NEFAZODONE HYDROCHLORIDE

Sponsor: SUN PHARM INDS LTD

APPLICATION
ANDA076409
TYPE
ANDA
ORIGINAL APPROVAL
2003-09-16
LATEST ACTION
2009-06-22
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

NEFAZODONE HYDROCHLORIDEDiscontinued
NEFAZODONE HYDROCHLORIDE 200MG · TABLET · ORAL
NEFAZODONE HYDROCHLORIDEDiscontinued
NEFAZODONE HYDROCHLORIDE 100MG · TABLET · ORAL
NEFAZODONE HYDROCHLORIDEDiscontinued
NEFAZODONE HYDROCHLORIDE 250MG · TABLET · ORAL
NEFAZODONE HYDROCHLORIDEDiscontinued
NEFAZODONE HYDROCHLORIDE 150MG · TABLET · ORAL
NEFAZODONE HYDROCHLORIDEDiscontinued
NEFAZODONE HYDROCHLORIDE 50MG · TABLET · ORAL

Approval history

2009-06-22Labeling · Supplement 5AP
2008-11-13Labeling · Supplement 4AP
2008-01-15Labeling · Supplement 2AP
2005-04-20Labeling · Supplement 1AP
2003-09-16Original — Other Important Information from FDA ↗AP
VIEW ON DRUGS@FDA ↗

Related on SPEQ

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Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.

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