vilazodone hydrochloride
- Product NDC
- 72205-262
- 11-digit product format
- 722050262
- Labeler code
- 72205
- Product ID
- 72205-262_c3e167cd-7f56-45eb-80df-a60fa1392e57
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vilazodone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Novadoz Pharmaceuticals LLC
- Application
- ANDA208228
- Marketing category
- ANDA
- Marketing start
- 2023-07-07
- Substance
- VILAZODONE HYDROCHLORIDE
- Active strength
- 40 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 | 40 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 |
|---|
| 72205-262-30 | vilazodone hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72205-262 | VILAZODONE HYDROCHLORIDE TABLET [NOVADOZ PHARMACEUTICALS LLC] | 1 | Current NDC, 1 package rows | 20230930_c3e167cd-7f56-45eb-80df-a60fa1392e57.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72205-262-30 | 72205026230 | 30 TABLET in 1 BOTTLE (72205-262-30) | 30 tablet | 2023-07-14 | No | No | Historical |