Finasteride NDC# 82187-1003-1 Container Description: The product packed in white poly bag… recall
FDA recall D-0262-2025 · initiated Feb 7, 2025
Aspen Biopharma Labs Pvt., Ltd. recalled Finasteride NDC# 82187-1003-1 Container Description: The product packed in whit… in Feb 2025 — an FDA Class II recall (D-0262-2025) because CGMP Deviations.
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
CGMP Deviations
The manufacturing process itself
The FDA found the process itself out of compliance, usually before any defective product was identified.
This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.
Is your product affected? Check the lot number
A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.
Quantity recalled: 120.0 kg
Details
- Product
- 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 company
- Aspen Biopharma Labs Pvt., Ltd.
- Classification
- Class II
- Status
- Ongoing
- Type
- Voluntary: Firm initiated
- Distribution
- Product was distributed to 3 distributors (1 Hong Kong and 2 accounts in Florida)
- Initiated
- Feb 7, 2025
- FDA report date
- Mar 19, 2025
Frequently asked
- Was Finasteride NDC# 82187-1003-1 Container Description: The product packed in whit… recalled?
- Aspen Biopharma Labs Pvt., Ltd. recalled Finasteride NDC# 82187-1003-1 Container Description: The product packed in whit… in Feb 2025 — an FDA Class II recall (D-0262-2025) because CGMP Deviations. May cause temporary or medically reversible harm; low probability of serious harm.
- Why was Finasteride NDC# 82187-1003-1 Container Description: The product packed in whit… recalled?
- Per the FDA enforcement record, the reason for recall D-0262-2025 was: CGMP Deviations
- Is a recalled Finasteride NDC# 82187-1003-1 Container Description: The product packed in whit… dangerous to take?
- An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
- Which lots of Finasteride NDC# 82187-1003-1 Container Description: The product packed in whit… are affected?
- Distributed: Product was distributed to 3 distributors (1 Hong Kong and 2 accounts in Florida). The recall covers these lots — Lot Numbers: HAFSC0040923, exp. date Aug-2027 HAFSC0050923, exp. date Aug-2027. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0262-2025.