FdaApplication
ANDA 078163
Identifiers
- fda_app_no: ANDA078163
Properties
| Property | Value |
|---|---|
| applicant_name | ORBION PHARMACEUTICALS PRIVATE LTD |
| application_type | ANDA |
| approval_date | 2007-07-02 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TERBINAFINE HYDROCHLORIDE | TERBINAFINE HYDROCHLORIDE | EQ 250MG BASE | TABLET;ORAL |
1 product