FdaApplication
ANDA 075089
Identifiers
- fda_app_no: ANDA075089
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 1999-07-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TICLOPIDINE HYDROCHLORIDE | TICLOPIDINE HYDROCHLORIDE | 250MG | TABLET;ORAL |
1 product