FdaApplication
ANDA 089042
Identifiers
- fda_app_no: ANDA089042
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1985-10-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROCAINAMIDE HYDROCHLORIDE | PROCAINAMIDE HYDROCHLORIDE | 750MG | TABLET, EXTENDED RELEASE;ORAL |
1 product