FdaApplication
NDA 022152
Identifiers
- fda_app_no: NDA022152
Properties
| Property | Value |
|---|---|
| applicant_name | BIONPHARMA INC |
| application_type | NDA |
| approval_date | 2008-07-29 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| STAVZOR | VALPROIC ACID | 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE, DELAYED RELEASE;ORAL |
| STAVZOR | VALPROIC ACID | 250MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE, DELAYED RELEASE;ORAL |
| STAVZOR | VALPROIC ACID | 125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE, DELAYED RELEASE;ORAL |
3 products