FdaApplication
ANDA 078962
Identifiers
- fda_app_no: ANDA078962
Properties
| Property | Value |
|---|---|
| applicant_name | KVK TECH INC |
| application_type | ANDA |
| approval_date | 2008-06-27 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BETAXOLOL HYDROCHLORIDE | BETAXOLOL HYDROCHLORIDE | 10MG | TABLET;ORAL |
| BETAXOLOL HYDROCHLORIDE | BETAXOLOL HYDROCHLORIDE | 20MG | TABLET;ORAL |
2 products