US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 2, 2022 (4 years ago)

Losartan HCTZ 100/25 mg, 90 count bottles NDC# 70518-2578-00 Repackaged NDC Original…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.

What was recalled

Losartan HCTZ 100/25 mg, 90 count bottles NDC# 70518-2578-00 Repackaged NDC Original NDC # 68180-0217-09

Recalling firm
RemedyRepack Inc.
NDC code
70518-2578-00
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0886-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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