NDC 68788-8774
Venlafaxine Hydrochloride 150 mg capsule, extended release
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 70710-1700.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA090174
- On the market since
- Nov 20, 2024
- Package NDCs
68788-8774-168788-8774-268788-8774-368788-8774-668788-8774-868788-8774-9- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?