RecallHawk

CETIRIZINE HCL

BIONPHARMA

Summary

FDA approved CETIRIZINE HCL by BIONPHARMA. NDA (New Drug) approval (Labeling) on 2026-01-30. CAPSULE, ORAL.

Details

Source

Drug Approval

External ID

NDA022429-26

Action Date

2026-01-30

Status

Approved

Category

drug

Product Code

NDA (New Drug)

Product Description

CETIRIZINE HCL, CAPSULE, ORAL. Application: NDA022429

Company

Context & Analysis

BIONPHARMA has 27 FDA actions in our database.

Frequently Asked Questions

How often does BIONPHARMA have FDA actions?

BIONPHARMA has 27 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 "NDA022429-26" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for drug

Related Actions