← FDA Drug Approvals (Drugs@FDA)
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
- Machine
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