NDC 69367-417 – Venlafaxine Hydrochloride
Venlafaxine Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral
Product NDC69367-417
Product details
- Brand name
- Venlafaxine Hydrochloride
- Generic name
- Venlafaxine Hydrochloride
- Labeler
- Westminster Pharmaceuticals, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205468
- Marketed since
- November 18, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin and Norepinephrine Reuptake Inhibitor
Active ingredients
- Venlafaxine Hydrochloride 150 mg/1
Uses, dosage, side effects and warnings for Venlafaxine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 69367-417-09 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-09) | Nov 18, 2025 |
| 69367-417-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-30) | Nov 18, 2025 |
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