FdaApplication
ANDA 040676
Identifiers
- fda_app_no: ANDA040676
Properties
| Property | Value |
|---|---|
| applicant_name | MIKART LLC |
| application_type | ANDA |
| approval_date | 2006-04-19 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE AND ACETAMINOPHEN | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 500MG;10MG | TABLET;ORAL |
1 product