NDC 72189-066
Venlafaxine Hydrochloride 150 mg capsule, extended release
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Aurobindo Pharma Limited's NDC 65862-697.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it
Recalls
- Dec 22, 2016 · Class II · Aurobindo Pharma USA Inc
Failed Tablet/Capsule Specifications: Some bottles contain punctured, and/or clumped/melted capsules.
Lots: Lot #: VI3716010-A, Exp. 04/2018
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Venlafaxine: every company that makes it
- Form
- capsule, extended release
- Strength
- 150 mg
- Approval
- ANDA ANDA200834
- On the market since
- Jan 7, 2020
- Package NDCs
72189-066-30- Official label
- DailyMed (National Library of Medicine), updated Jan 7, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?