NDC 35208-012
Venlafaxine Hydrochloride 75 mg capsule, extended release
On the label: IntelliPharmaCeutics Corp..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| IntelliPharmaCeutics Corp. | Location not on file | Makes it and packages it | Not inspected on record |
| Moehs Cantabra SL | Polanco, Spain | Makes the active ingredient | Problems found, fixed voluntarilyJul 17, 2025 · 6 inspections, 1 with FDA action |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release
- Strength
- 75 mg
- Approval
- ANDA ANDA201272
- On the market since
- Dec 3, 2018
- Package NDCs
35208-012-1035208-012-15- Official label
- DailyMed (National Library of Medicine), updated Oct 9, 2018
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