NDC 69367-417
Venlafaxine Hydrochloride 150 mg tablet, extended release
On the label: Westminster Pharmaceuticals, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| MPP Pharma LLC | Kansas City, MO, United States | Makes it, tests it, packages it and labels it | Serious problems, FDA actionApr 2, 2026 · 12 inspections, 4 with FDA action |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA205468
- On the market since
- Nov 18, 2025
- Package NDCs
69367-417-0969367-417-30- Official label
- DailyMed (National Library of Medicine), updated Nov 25, 2025
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