NDC 70518-4566
Venlafaxine 75 mg tablet, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 70710-1349.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyMar 24, 2023 · 5 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 75 mg
- Approval
- ANDA ANDA215622
- On the market since
- Feb 4, 2026
- Package NDCs
70518-4566-0- Official label
- DailyMed (National Library of Medicine), updated Feb 5, 2026
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