FdaApplication
ANDA 207574
Identifiers
- fda_app_no: ANDA207574
Properties
| Property | Value |
|---|---|
| applicant_name | SANALUZ LLC |
| application_type | ANDA |
| approval_date | 2016-12-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE AND ACETAMINOPHEN | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 325MG;5MG | TABLET;ORAL |
1 product