NDC 80425-0581
Venlafaxine Hydrochloride 37.5 mg capsule, extended release
On the label: Advanced Rx Pharmacy of Tennessee, LLC. It's repackaged: Advanced Rx Pharmacy of Tennessee, LLC rebottles it from Granules Pharmaceuticals Inc.'s NDC 70010-184.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Granules India Limited | Medchal-Malkajgiri District, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyFeb 14, 2020 · 6 inspections |
Repackaging site
- Advanced Rx Pharmacy of Tennessee, LLC, Nashville, TN, United States · repackages it
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA217390
- On the market since
- Apr 9, 2026
- Package NDCs
80425-0581-180425-0581-280425-0581-3- Official label
- DailyMed (National Library of Medicine), updated Apr 9, 2026
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