RecallHawk

ZEVTERA (CEFTOBIPROLE MEDOCARIL SODIUM)

ISTX

Summary

FDA approved ZEVTERA (CEFTOBIPROLE MEDOCARIL SODIUM) by ISTX. NDA (New Drug) approval (Labeling) on 2026-06-26. POWDER, INTRAVENOUS.

Details

Source

Drug Approval

External ID

NDA218275-1

Action Date

2026-06-26

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

ZEVTERA (generic: CEFTOBIPROLE MEDOCARIL SODIUM), POWDER, INTRAVENOUS. Application: NDA218275

Company

Context & Analysis

Frequently Asked Questions

How often does ISTX have FDA actions?

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

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "NDA218275-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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