NDC 51655-323
venlafaxine 37.5 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-173.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA090555
- On the market since
- May 2, 2023
- Package NDCs
51655-323-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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