FdaApplication
ANDA 071059
Identifiers
- fda_app_no: ANDA071059
Properties
| Property | Value |
|---|---|
| applicant_name | ALRA LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1988-08-11 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBU-TAB | IBUPROFEN | 600MG | TABLET;ORAL |
1 product