FdaApplication
ANDA 202160
Identifiers
- fda_app_no: ANDA202160
Properties
| Property | Value |
|---|---|
| applicant_name | AUROLIFE PHARMA LLC |
| application_type | ANDA |
| approval_date | 2012-11-19 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | 30MG | TABLET;ORAL |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | 15MG | TABLET;ORAL |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | 5MG | TABLET;ORAL |
3 products