FdaApplication
ANDA 075678
Identifiers
- fda_app_no: ANDA075678
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS ELIZABETH LLC |
| application_type | ANDA |
| approval_date | 2000-07-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PEMOLINE | PEMOLINE | 37.5MG | TABLET, CHEWABLE;ORAL |
1 product