FdaApplication
ANDA 089369
Identifiers
- fda_app_no: ANDA089369
Properties
| Property | Value |
|---|---|
| applicant_name | ANI PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 1987-01-09 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROCAINAMIDE HYDROCHLORIDE | PROCAINAMIDE HYDROCHLORIDE | 750MG | TABLET, EXTENDED RELEASE;ORAL |
| PROCAINAMIDE HYDROCHLORIDE | PROCAINAMIDE HYDROCHLORIDE | 500MG | TABLET, EXTENDED RELEASE;ORAL |
| PROCAINAMIDE HYDROCHLORIDE | PROCAINAMIDE HYDROCHLORIDE | 250MG | TABLET, EXTENDED RELEASE;ORAL |
3 products