FdaApplication
ANDA 203823
Identifiers
- fda_app_no: ANDA203823
Properties
| Property | Value |
|---|---|
| applicant_name | LANNETT CO INC |
| application_type | ANDA |
| approval_date | 2014-08-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE HYDROCHLORIDE | OXYCODONE HYDROCHLORIDE | 5MG | CAPSULE;ORAL |
1 product