NDC 70518-3971
Venlafaxine Hydrochloride 37.5 mg capsule, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Epic Pharma, LLC's NDC 42806-601.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Yichang Humanwell Oral Solid Dosage Plant | Yichang, China | Makes it | No problems foundJul 21, 2023 · 2 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA214654
- On the market since
- Dec 27, 2023
- Package NDCs
70518-3971-0- Official label
- DailyMed (National Library of Medicine), updated Jun 11, 2026
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