RecallHawk

GVOKE HYPOPEN 0.5 MG AUTO-INJECTOR (GLUCAGON INJECTION, SOLUTION)

XERIS

Summary

FDA approved GVOKE HYPOPEN 0.5 MG AUTO-INJECTOR (GLUCAGON INJECTION, SOLUTION) by XERIS. NDA (New Drug) approval (Efficacy) on 2025-03-14. SOLUTION, SUBCUTANEOUS.

Details

Source

Drug Approval

External ID

NDA212097-12

Action Date

2025-03-14

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

GVOKE HYPOPEN 0.5 MG AUTO-INJECTOR (generic: GLUCAGON INJECTION, SOLUTION), SOLUTION, SUBCUTANEOUS. Application: NDA212097

Company

Context & Analysis

Frequently Asked Questions

How often does XERIS have FDA actions?

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

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "NDA212097-12" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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