FdaApplication
ANDA 207333
Identifiers
- fda_app_no: ANDA207333
Properties
| Property | Value |
|---|---|
| applicant_name | LANNETT CO INC |
| application_type | ANDA |
| approval_date | 2017-09-25 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE AND ACETAMINOPHEN | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 325MG;10MG | TABLET;ORAL |
| OXYCODONE AND ACETAMINOPHEN | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 325MG;5MG | TABLET;ORAL |
2 products