Vilazodone Hydrochloride
- Product NDC
- 51407-916
- 11-digit product format
- 514070916
- Labeler code
- 51407
- Product ID
- 51407-916_3b8c8c08-ce7c-b237-e063-6294a90aeb14
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Vilazodone Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA208212
- Marketing category
- ANDA
- Marketing start
- 2019-09-30
- Substance
- VILAZODONE HYDROCHLORIDE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| U8HTX2GK8J | VILAZODONE HYDROCHLORIDE | 163521-08-2 | VILAZODONE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 51407-916-30 | 51407091630 | 30 TABLET, FILM COATED in 1 BOTTLE (51407-916-30) | 2025-05-27 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Vilazodone Hydrochloride | Golden State Medical Supply, Inc. | 2025-08-04 | HUMAN PRESCRIPTION DRUG LABEL | 1 |