FdaApplication
ANDA 071027
Identifiers
- fda_app_no: ANDA071027
Properties
| Property | Value |
|---|---|
| applicant_name | HALSEY DRUG CO INC |
| application_type | ANDA |
| approval_date | 1987-09-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 200MG | TABLET;ORAL |
1 product