FdaApplication
ANDA 075998
Identifiers
- fda_app_no: ANDA075998
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | ANDA |
| approval_date | 2001-11-29 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROPAFENONE HYDROCHLORIDE | PROPAFENONE HYDROCHLORIDE | 225MG | TABLET;ORAL |
| PROPAFENONE HYDROCHLORIDE | PROPAFENONE HYDROCHLORIDE | 300MG | TABLET;ORAL |
| PROPAFENONE HYDROCHLORIDE | PROPAFENONE HYDROCHLORIDE | 150MG | TABLET;ORAL |
3 products