FdaApplication
ANDA 088959
Identifiers
- fda_app_no: ANDA088959
Properties
| Property | Value |
|---|---|
| applicant_name | ANI PHARMACEUTICALS INC |
| application_type | ANDA |
| approval_date | 1985-12-02 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROCAINAMIDE HYDROCHLORIDE | PROCAINAMIDE HYDROCHLORIDE | 500MG | TABLET, EXTENDED RELEASE;ORAL |
1 product