NDC 70771-1836
Venlafaxine Hydrochloride 37.5 mg capsule, extended release
On the label: Cadila Healthcare Limited.
Where it's 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 |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA090174
- On the market since
- May 18, 2023
- Package NDCs
70771-1836-070771-1836-270771-1836-370771-1836-470771-1836-570771-1836-9- Official label
- DailyMed (National Library of Medicine), updated May 19, 2023
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