FdaApplication
ANDA 090070
Identifiers
- fda_app_no: ANDA090070
Properties
| Property | Value |
|---|---|
| applicant_name | DOCTOR REDDYS LABORATORIES LTD |
| application_type | ANDA |
| approval_date | 2012-03-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DIVALPROEX SODIUM | DIVALPROEX SODIUM | EQ 500MG VALPROIC ACID | TABLET, EXTENDED RELEASE;ORAL |
1 product