NDC 43598-944 – Venlafaxine
Venlafaxine Hydrochloride 225 mg/1 · Tablet, Extended Release · Oral
Product NDC43598-944
Product details
- Brand name
- Venlafaxine
- Generic name
- Venlafaxine
- Labeler
- Dr. Reddy's Laboratories Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA214609
- Marketed since
- September 20, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 225 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 43598-944-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-30) | Sep 20, 2021 |
| 43598-944-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43598-944-90) | Sep 20, 2021 |
Recalls mentioning this NDC
- D-0208-2025 Jan 29, 2025 · Class III
Failed Tablet/Capsule Specifications: Missing tab ID on either side of the tablet
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