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SURFAXIN

NDA · New Drug Application · Sponsor: LEES PHARM HK · Approved 2012-03-06

Drug application

FDA Application #
NDA021746
Application type
New Drug Application
Brand name
SURFAXIN
Generic name
Lucinactant
Active ingredients
LUCINACTANT
Dosage form
SUSPENSION
Route
INTRATRACHEAL
Marketing status
Discontinued
Sponsor
LEES PHARM HK
First approval
2012-03-06

Source

Authoritative
Drugs@FDA application overview
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