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VORTIOXETINE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: PRINSTON PHARMA INC · Approved 2022-07-28

Drug application

FDA Application #
ANDA211024
Application type
Abbreviated New Drug Application (Generic)
Brand name
VORTIOXETINE
Generic name
Vortioxetine
Active ingredients
VORTIOXETINE
Dosage form
TABLET
Route
ORAL
Marketing status
None (Tentative Approval)
Sponsor
PRINSTON PHARMA INC
First approval
2022-07-28

Source

Authoritative
Drugs@FDA application overview
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