NDC 51655-489
Glimepiride 4 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-322.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
| Dr. Reddy's Laboratories Limited | Srikakulam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 20, 2022 · 5 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Jan 18, 2024 · Class III · Dr. Reddy's Laboratories, Inc.
Misprint on tablet
Lots: Lot: T2303622; Exp. 06/2026 Lot: T2303626; Exp. 06/2026 Lot: T2303627; Exp. 06/2026 Lot: T2303628; Exp. 06/2026 Lot: T2303629; Exp. 06/2026 - Jan 18, 2024 · Class III · Dr. Reddy's Laboratories, Inc.
Misprint on tablet
Lots: Lot: T2303609; Exp. 06/2026 Lot: T2303610; Exp. 06/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Glimepiride: every company that makes it
- Form
- tablet, oral
- Strength
- 4 mg
- Approval
- ANDA ANDA077091
- On the market since
- Dec 10, 2020
- Package NDCs
51655-489-2651655-489-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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