NDC 55111-453
venlafaxine hydrochloride 37.5 mg capsule, extended release
On the label: Dr.Reddy's Laboratories Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA078421
- On the market since
- Jun 1, 2011
- Package NDCs
55111-453-0155111-453-0555111-453-3055111-453-6055111-453-7855111-453-7955111-453-90- Official label
- DailyMed (National Library of Medicine), updated Dec 6, 2018
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