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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Vilazodone Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VILAZODONE HYDROCHLORIDE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | U8HTX2GK8J |
| Rxcui | 1086772, 1086778, 1086784 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-916-30 | Vilazodone Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |