RecallHawk

MESALAMINE

TEVA PHARMS INC

Summary

FDA approved MESALAMINE by TEVA PHARMS INC. ANDA (Generic) approval on 2024-08-22. TABLET, DELAYED RELEASE, ORAL.

Details

Source

Drug Approval

External ID

ANDA213191-1

Action Date

2024-08-22

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

MESALAMINE, TABLET, DELAYED RELEASE, ORAL. Application: ANDA213191

Context & Analysis

TEVA PHARMS INC has 7 FDA actions in our database.

Frequently Asked Questions

How often does TEVA PHARMS INC have FDA actions?

TEVA PHARMS INC has 7 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 "ANDA213191-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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