RecallHawk

LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

HETERO LABS LTD V

Summary

FDA approved LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE by HETERO LABS LTD V. ANDA (Generic) approval on 2026-05-27. TABLET, ORAL.

Details

Source

Drug Approval

External ID

ANDA219869-1

Action Date

2026-05-27

Status

Approved

Category

drug

Product Code

ANDA (Generic)

Product Description

LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, TABLET, ORAL. Application: ANDA219869

Context & Analysis

HETERO LABS LTD V has 27 FDA actions in our database.

Frequently Asked Questions

How often does HETERO LABS LTD V have FDA actions?

HETERO LABS LTD V 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 "ANDA219869-1" 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