Venlafaxine Hydrochloride
- Product NDC
- 50090-7940
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Venlafaxine Hydrochloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA200834
- Marketing category
- ANDA
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7940-0 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7940-0) | 2026-03-18 | | No | Historical |
| 50090-7940-1 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7940-1) | 2026-03-18 | | No | Historical |
| 50090-7940-2 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7940-2) | 2026-03-18 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine Hydrochloride | A-S Medication Solutions | 2026-03-23 | Human Prescription Drug Label | 1 |