US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Feb 7, 2025 (2 years ago)

Finasteride NDC# 82187-1003-1 Container Description: The product packed in white poly…

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

Why it was recalled

CGMP Deviations

What was recalled

Finasteride NDC# 82187-1003-1 Container Description: The product packed in white poly bag containing black poly bag and tied each individual finally packed in HDPE container for shipping.

Recalling firm
Aspen Biopharma Labs Pvt., Ltd.
NDC code
82187-1003-1
Origin
India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0262-2025

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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