NDC 60687-607
Desvenlafaxine 50 mg tablet, film coated, extended release
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0054-0400.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| West-Ward Columbus Inc. | Columbus, OH, United States | Makes it | No problems foundApr 30, 2026 · 27 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Desvenlafaxine: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA204082
- On the market since
- Dec 1, 2021
- Package NDCs
60687-607-1160687-607-21- Official label
- DailyMed (National Library of Medicine), updated Oct 10, 2024
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