NDC 70518-1385
venlafaxine 37.5 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-173.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA090555
- On the market since
- Aug 24, 2018
- Package NDCs
70518-1385-070518-1385-170518-1385-270518-1385-3- Official label
- DailyMed (National Library of Medicine), updated Jul 6, 2026
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