RecallHawk

VOQUEZNA TRIPLE PAK (VONOPRAZAN FUMARATE, AMOXICILLIN AND CLARITHROMYCIN)

PHATHOM

Summary

FDA approved VOQUEZNA TRIPLE PAK (VONOPRAZAN FUMARATE, AMOXICILLIN AND CLARITHROMYCIN) by PHATHOM. NDA (New Drug) approval (Labeling) on 2025-10-31. CAPSULE, TABLET, TABLET, ORAL.

Details

Source

Drug Approval

External ID

NDA215152-12

Action Date

2025-10-31

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

VOQUEZNA TRIPLE PAK (generic: VONOPRAZAN FUMARATE, AMOXICILLIN AND CLARITHROMYCIN), CAPSULE, TABLET, TABLET, ORAL. Application: NDA215152

Company

Context & Analysis

PHATHOM has 3 FDA actions in our database.

Frequently Asked Questions

How often does PHATHOM have FDA actions?

PHATHOM has 3 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 "NDA215152-12" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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