NDC 72603-747
Venlafaxine Hydrochloride 37.5 mg capsule, extended release
On the label: Northstar Rx LLC..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alembic Pharmaceuticals Limited | Panchmahal, India | Makes it | No problems foundJul 26, 2024 · 8 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA217767
- On the market since
- Jun 1, 2026
- Package NDCs
72603-747-01- Official label
- DailyMed (National Library of Medicine), updated May 22, 2026
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