RecallHawk

DIVALPROEX SODIUM

DR REDDYS LABS LTD

Summary

FDA approved DIVALPROEX SODIUM by DR REDDYS LABS LTD. ANDA (Generic) approval (Labeling) on 2024-07-10. TABLET, EXTENDED RELEASE, ORAL.

Details

Source

Drug Approval

External ID

ANDA090161-25

Action Date

2024-07-10

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

DIVALPROEX SODIUM, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA090161

Context & Analysis

DR REDDYS LABS LTD has 15 FDA actions in our database.

Frequently Asked Questions

How often does DR REDDYS LABS LTD have FDA actions?

DR REDDYS LABS LTD has 15 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA090161-25" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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