NDC 61919-882
Desvenlafaxine ER 50 mg tablet, film coated, extended release
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-592.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Repackaging site
- Direct Rx, Dawsonville, GA, 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 ANDA204172
- On the market since
- Jun 4, 2019
- Package NDCs
61919-882-2861919-882-3061919-882-60- Official label
- DailyMed (National Library of Medicine), updated Mar 5, 2026
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