FdaApplication
ANDA 076741
Identifiers
- fda_app_no: ANDA076741
Properties
| Property | Value |
|---|---|
| applicant_name | LNK INTERNATIONAL INC |
| application_type | ANDA |
| approval_date | 2004-06-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 100MG | TABLET;ORAL |
1 product