FdaApplication
ANDA 074879
Identifiers
- fda_app_no: ANDA074879
Properties
| Property | Value |
|---|---|
| applicant_name | ALKERMES GAINESVILLE LLC |
| application_type | ANDA |
| approval_date | 1997-12-10 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| KETOPROFEN | KETOPROFEN | 200MG | CAPSULE, EXTENDED RELEASE;ORAL |
1 product