NDC 70518-4632
Venlafaxine Hydrochloride 75 mg capsule, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Granules Pharmaceuticals Inc.'s NDC 70010-185.
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 |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 75 mg
- Approval
- ANDA ANDA217390
- On the market since
- Apr 24, 2026
- Package NDCs
70518-4632-0- Official label
- DailyMed (National Library of Medicine), updated Apr 28, 2026
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