NDC 82868-035
Glipizide 10 mg tablet, extended release
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Aurobindo Pharma Limited's NDC 59651-782.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Glipizide: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA206928
- On the market since
- Jan 9, 2024
- Package NDCs
82868-035-3082868-035-90- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2025
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