FdaApplication
ANDA 217358
Identifiers
- fda_app_no: ANDA217358
Properties
| Property | Value |
|---|---|
| applicant_name | MANKIND PHARMA LTD |
| application_type | ANDA |
| approval_date | 2025-08-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DIVALPROEX SODIUM | DIVALPROEX SODIUM | EQ 125MG VALPROIC ACID | CAPSULE, DELAYED REL PELLETS;ORAL |
1 product