RecallHawk

ISOSORBIDE MONONITRATE

ZYDUS PHARMS

Summary

FDA approved ISOSORBIDE MONONITRATE by ZYDUS PHARMS. ANDA (Generic) approval on 2024-02-15. TABLET, EXTENDED RELEASE, ORAL.

Details

Source

Drug Approval

External ID

ANDA218255-1

Action Date

2024-02-15

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

ISOSORBIDE MONONITRATE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA218255

Context & Analysis

ZYDUS PHARMS has 60 FDA actions in our database.

Frequently Asked Questions

How often does ZYDUS PHARMS have FDA actions?

ZYDUS PHARMS has 60 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 "ANDA218255-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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