NDC 72865-199
Venlafaxine Hydrochloride 150 mg tablet, extended release
On the label: XLCare Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ascent Pharmaceuticals Inc | Central Islip, NY, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA214419
- On the market since
- Feb 26, 2021
- Package NDCs
72865-199-3072865-199-90- Official label
- DailyMed (National Library of Medicine), updated Oct 29, 2021
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