NDC 70518-2532
Venlafaxine Hydrochloride 37.5 mg capsule, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-527.
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 |
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, oral
- Strength
- 37.5 mg
- Approval
- ANDA ANDA200834
- On the market since
- Jan 8, 2020
- Package NDCs
70518-2532-070518-2532-170518-2532-270518-2532-370518-2532-470518-2532-5- Official label
- DailyMed (National Library of Medicine), updated Jul 8, 2026
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