NDC 71921-172
Venlafaxine Hydrochloride 37.5 mg capsule, extended release
On the label: Florida Pharmaceutical Products, LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Inventia Healthcare Limited | Thane, India | Makes it | Problems found, fixed voluntarilyFeb 12, 2025 · 4 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release
- Strength
- 37.5 mg
- Approval
- ANDA ANDA203332
- On the market since
- Mar 20, 2020
- Package NDCs
71921-172-0371921-172-09- Official label
- DailyMed (National Library of Medicine), updated Dec 20, 2022
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