FdaApplication
ANDA 090500
Identifiers
- fda_app_no: ANDA090500
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2014-04-04 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VALACYCLOVIR HYDROCHLORIDE | VALACYCLOVIR HYDROCHLORIDE | EQ 1GM BASE | TABLET;ORAL |
| VALACYCLOVIR HYDROCHLORIDE | VALACYCLOVIR HYDROCHLORIDE | EQ 500MG BASE | TABLET;ORAL |
2 products