NDC 33342-194
Venlafaxine hydrochloride 37.5 mg capsule, extended release
On the label: Macleods Pharmaceuticals Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Macleods Pharmaceuticals Limited | District Solan, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA204889
- On the market since
- Oct 6, 2017
- Package NDCs
33342-194-0733342-194-1033342-194-1133342-194-15- Official label
- DailyMed (National Library of Medicine), updated May 15, 2026
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