Reported May 31, 2023 · Terminated
Glimepiride Tablets, USP, 1 mg, RX, Packaged as a)100-count bottle, NDC# 68001-177-00; b) 500-count bottle, NDC#…
Amerisource Health Services LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Amerisource Health Services LLC · 2550 John Glenn Ave Ste A · Columbus, OH · 43217-1188
Is this the product you have?
Glimepiride TabletsUSP1 mgRXPackaged as a)100-count bottleNDC# 68001-177-00b) 500-count bottleNDC# 68001-177-03
- Manufactured byIntas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213. INDIA. For BluePoint Laboratories
- Lot codes and dates
10 of 10 products
Products covered by this recall # Product as published 1 Batches a) P2002616, EXP 04/30/2023 2 P2006509, EXP 11/30/2023 3 P2103572, EXP 04/30/2024 4 P2106811, EXP 09/30/2024 5 R2200578, EXP 04/30/2025 b)P2100095, EXP 11/30/2023 6 P2100624, EXP 01/31/2024 7 P2101780, EXP 02/29/2024 8 P2107383, EXP 09/30/2024 9 P2201505, EXP 02/28/2025 10 R2201109, EXP 06/30/2025 - Amount recalled
- 63,335 bottles
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
CGMP Deviations: recalling drug products following an FDA inspection.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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