NDC 47335-794
Venlafaxine Hydrochloride 225 mg tablet, extended release
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Halol, India | Makes it and tests it | Serious problems, FDA actionJun 13, 2025 · 12 inspections, 5 with FDA action |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 225 mg
- Approval
- ANDA ANDA091272
- On the market since
- Feb 15, 2019
- Package NDCs
47335-794-0847335-794-1347335-794-8147335-794-8347335-794-8847335-794-99- Official label
- DailyMed (National Library of Medicine), updated Sep 15, 2023
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