NDC 43598-999
venlafaxine hydrochloride 37.5 mg capsule, extended release
On the label: Dr. Reddy's Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Srikakulam, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 20, 2022 · 5 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA078421
- On the market since
- Sep 9, 2024
- Package NDCs
43598-999-1043598-999-3043598-999-90- Official label
- DailyMed (National Library of Medicine), updated Mar 26, 2025
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