RecallHawk

CETIRIZINE HYDROCHLORIDE

BAJAJ

Summary

FDA approved CETIRIZINE HYDROCHLORIDE by BAJAJ. ANDA (Generic) approval (Manufacturing (CMC)) on 2025-08-29. SOLUTION, ORAL.

Details

Source

Drug Approval

External ID

ANDA090191-10

Action Date

2025-08-29

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

CETIRIZINE HYDROCHLORIDE, SOLUTION, ORAL. Application: ANDA090191

Company

Context & Analysis

Frequently Asked Questions

How often does BAJAJ have FDA actions?

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

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "ANDA090191-10" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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