FdaApplication
ANDA 072137
Identifiers
- fda_app_no: ANDA072137
Properties
| Property | Value |
|---|---|
| applicant_name | HALSEY DRUG CO INC |
| application_type | ANDA |
| approval_date | 1988-02-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 800MG | TABLET;ORAL |
1 product