FdaApplication
ANDA 075191
Identifiers
- fda_app_no: ANDA075191
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 1999-06-09 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PENTOXIFYLLINE | PENTOXIFYLLINE | 400MG | TABLET, EXTENDED RELEASE;ORAL |
1 product