NDC 43598-943
Venlafaxine 150 mg tablet, extended release
On the label: Dr. Reddy's Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Appco Pharma LLC | Piscataway, NJ, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections |
Recalls
- Jan 16, 2025 · Class III · Appco Pharma LLC
Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet
Lots: Lot #: 2402101UR, Exp 02/28/2027
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
- tablet, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA214609
- On the market since
- Sep 20, 2021
- Package NDCs
43598-943-3043598-943-90- Official label
- DailyMed (National Library of Medicine), updated Oct 6, 2023
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