NDC 68001-496
Venlafaxine Hydrochloride 37.5 mg tablet, extended release
On the label: BluePoint Laboratories..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ascent Pharmaceuticals Inc | Central Islip, NY, United States | Makes it, tests it, packages it and labels 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
- 37.5 mg
- Approval
- ANDA ANDA214419
- On the market since
- Apr 30, 2021
- Package NDCs
68001-496-0468001-496-05- Official label
- DailyMed (National Library of Medicine), updated Jan 10, 2025
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