NDC 29033-046
Venlafaxine Hydrochloride 225 mg tablet, extended release
On the label: Nostrum Laboratories, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Nostrum Laboratories, Inc. | Bryan, Ohio, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMar 13, 2025 · 6 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet, extended release
- Strength
- 225 mg
- Approval
- ANDA ANDA205468
- On the market since
- Mar 27, 2017
- Package NDCs
29033-046-3029033-046-90- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2018
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