Venlafaxine Hydrochloride
- Product NDC
- 50090-7323
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VENLAFAXINE HYDROCHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA214654
- Marketing category
- ANDA
- Substance
- VENLAFAXINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7323-0 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7323-0) | 2024-10-15 | | No | Historical |
| 50090-7323-1 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-7323-1) | 2024-10-15 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Venlafaxine Hydrochloride | A-S Medication Solutions | 2025-12-01 | HUMAN PRESCRIPTION DRUG LABEL | 3 |