RecallHawk

VANCOMYCIN HYDROCHLORIDE

XELLIA PHARMS APS

Summary

FDA approved VANCOMYCIN HYDROCHLORIDE by XELLIA PHARMS APS. ANDA (Generic) approval (Labeling) on 2021-09-24. INJECTABLE, INJECTION.

Details

Source

Drug Approval

External ID

ANDA204125-11

Action Date

2021-09-24

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

VANCOMYCIN HYDROCHLORIDE, INJECTABLE, INJECTION. Application: ANDA204125

Context & Analysis

XELLIA PHARMS APS has 4 FDA actions in our database.

Frequently Asked Questions

How often does XELLIA PHARMS APS have FDA actions?

XELLIA PHARMS APS has 4 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 "ANDA204125-11" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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