← FDA Drug Approvals (Drugs@FDA)
OXYCONTIN
NDA · New Drug Application · Sponsor: PURDUE PHARMA LP · Approved 2010-04-05
Drug application
- FDA Application #
NDA022272- Application type
- New Drug Application
- Brand name
- OXYCONTIN
- Generic name
- OXYCODONE HYDROCHLORIDE
- Active ingredients
- OXYCODONE HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- PURDUE PHARMA LP
- Manufacturer
- Knoa Pharma LLC
- First approval
- 2010-04-05
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown