NDC 67877-729 – Venlafaxine
Venlafaxine Hydrochloride 225 mg/1 · Tablet, Extended Release · Oral
Product NDC67877-729
Product details
- Brand name
- Venlafaxine
- Generic name
- Venlafaxine
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA214127
- Marketed since
- June 11, 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 |
|---|---|---|
| 67877-729-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-729-30) | Jun 11, 2021 |
| 67877-729-90 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-729-90) | Jun 11, 2021 |
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