FdaApplication
ANDA 089371
Identifiers
- fda_app_no: ANDA089371
Properties
| Property | Value |
|---|---|
| applicant_name | IDT AUSTRALIA LTD |
| application_type | ANDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROCAINAMIDE HYDROCHLORIDE | PROCAINAMIDE HYDROCHLORIDE | 750MG | TABLET, EXTENDED RELEASE;ORAL |
1 product