NDC 64980-581
Venlafaxine Hydrochloride 225 mg tablet, extended release
On the label: Rising Pharma Holdings, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Unique Pharmaceutical Laboratories | Bharuch, India | Makes it | Problems found, fixed voluntarilyOct 23, 2022 · 6 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 225 mg
- Approval
- ANDA ANDA216044
- On the market since
- Nov 28, 2022
- Package NDCs
64980-581-0364980-581-09- Official label
- DailyMed (National Library of Medicine), updated Apr 3, 2025
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