US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 10, 2020 (6 years ago)

BusPIRone Hydrochloride Tablets, USP 7.5 mg NDC# 49884-725-01

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

Why it was recalled

Failed Impurity /Degradation Specifications

What was recalled

BusPIRone Hydrochloride Tablets, USP 7.5 mg NDC# 49884-725-01

Recalling firm
Par Pharmaceutical Inc.
NDC code
49884-725-01
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1542-2020

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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