FdaApplication
ANDA 075189
Identifiers
- fda_app_no: ANDA075189
Properties
| Property | Value |
|---|---|
| applicant_name | IMPAX LABORATORIES INC |
| application_type | ANDA |
| approval_date | 2000-05-26 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NABUMETONE | NABUMETONE | 500MG | TABLET;ORAL |
| NABUMETONE | NABUMETONE | 750MG | TABLET;ORAL |
2 products