FdaApplication
ANDA 040679
Identifiers
- fda_app_no: ANDA040679
Properties
| Property | Value |
|---|---|
| applicant_name | MIKART LLC |
| application_type | ANDA |
| approval_date | 2006-05-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYCODONE AND ACETAMINOPHEN | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE | 400MG;2.5MG | TABLET;ORAL |
1 product