NDC 68071-5332
Desvenlafaxine 50 mg tablet, extended release
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Northstar Rx LLC.'s NDC 72603-556.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Rubicon Research Limited | Thane, India | Makes it, tests it, packages it and labels it | No problems foundMar 8, 2024 · 5 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Desvenlafaxine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA204028
- On the market since
- May 2, 2025
- Package NDCs
68071-5332-3- Official label
- DailyMed (National Library of Medicine), updated Oct 7, 2026
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