FdaApplication
ANDA 212429
Identifiers
- fda_app_no: ANDA212429
Properties
| Property | Value |
|---|---|
| applicant_name | AUROLIFE PHARMA LLC |
| application_type | ANDA |
| approval_date | 2020-01-27 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | 100MG/5ML | SOLUTION;ORAL |
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | 5MG/5ML | SOLUTION;ORAL |
2 products