FdaApplication
ANDA 090529
Identifiers
- fda_app_no: ANDA090529
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | ANDA |
| approval_date | 2011-12-30 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VERAPAMIL HYDROCHLORIDE | VERAPAMIL HYDROCHLORIDE | 120MG | TABLET, EXTENDED RELEASE;ORAL |
| VERAPAMIL HYDROCHLORIDE | VERAPAMIL HYDROCHLORIDE | 180MG | TABLET, EXTENDED RELEASE;ORAL |
| VERAPAMIL HYDROCHLORIDE | VERAPAMIL HYDROCHLORIDE | 240MG | TABLET, EXTENDED RELEASE;ORAL |
3 products