NDC 82009-056
Venlafaxine Hydrochloride 37.5 mg capsule, extended release
On the label: Quallent Pharmaceuticals Health LLC.
Where it's 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
- capsule, extended release, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA200834
- On the market since
- Nov 21, 2022
- Package NDCs
82009-056-10- Official label
- DailyMed (National Library of Medicine), updated May 24, 2024
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