FdaApplication
NDA 022272
Identifiers
- fda_app_no: NDA022272
Properties
| Property | Value |
|---|---|
| applicant_name | KNOA PHARMA LLC |
| application_type | NDA |
| approval_date | 2010-04-05 |
Products (7)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCONTIN | OXYCODONE HYDROCHLORIDE | 60MG | TABLET, EXTENDED RELEASE;ORAL |
| OXYCONTIN | OXYCODONE HYDROCHLORIDE | 30MG | TABLET, EXTENDED RELEASE;ORAL |
| OXYCONTIN | OXYCODONE HYDROCHLORIDE | 80MG | TABLET, EXTENDED RELEASE;ORAL |
| OXYCONTIN | OXYCODONE HYDROCHLORIDE | 40MG | TABLET, EXTENDED RELEASE;ORAL |
| OXYCONTIN | OXYCODONE HYDROCHLORIDE | 20MG | TABLET, EXTENDED RELEASE;ORAL |
| OXYCONTIN | OXYCODONE HYDROCHLORIDE | 15MG | TABLET, EXTENDED RELEASE;ORAL |
| OXYCONTIN | OXYCODONE HYDROCHLORIDE | 10MG | TABLET, EXTENDED RELEASE;ORAL |
7 products