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NEFAZODONE HYDROCHLORIDE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: WATSON LABS · Approved 2003-09-16

Drug application

FDA Application #
ANDA076073
Application type
Abbreviated New Drug Application (Generic)
Brand name
NEFAZODONE HYDROCHLORIDE
Generic name
Nefazodone Hydrochloride
Active ingredients
NEFAZODONE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Marketing status
Discontinued
Sponsor
WATSON LABS
First approval
2003-09-16

Source

Authoritative
Drugs@FDA application overview
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