RecallHawk

NEXIUM 24HR (ESOMEPRAZOLE MAGNESIUM)

ASTRAZENECA LP

Summary

FDA approved NEXIUM 24HR (ESOMEPRAZOLE MAGNESIUM) by ASTRAZENECA LP. NDA (New Drug) approval (Labeling) on 2022-09-06. TABLET, DELAYED RELEASE, ORAL.

Details

Source

Drug Approval

External ID

NDA207920-7

Action Date

2022-09-06

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

NEXIUM 24HR (generic: ESOMEPRAZOLE MAGNESIUM), TABLET, DELAYED RELEASE, ORAL. Application: NDA207920

Context & Analysis

Frequently Asked Questions

How often does ASTRAZENECA LP have FDA actions?

This is the only FDA action we have on record for ASTRAZENECA LP in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "NDA207920-7" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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