FdaApplication
ANDA 071214
Identifiers
- fda_app_no: ANDA071214
Properties
| Property | Value |
|---|---|
| applicant_name | OHM LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1986-12-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROHM | IBUPROFEN | 200MG | TABLET;ORAL |
1 product