vilazodone hydrochloride
- Product NDC
- 60505-4374
- 11-digit product format
- 605054374
- Labeler code
- 60505
- Product ID
- 60505-4374_cf01e721-c246-593a-b0f8-20e03347b9a1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vilazodone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA208228
- Marketing category
- ANDA
- Marketing start
- 2023-10-26
- 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 |
|---|
| 60505-4374-0 | vilazodone hydrochloride | 100 in 1 BLISTER PACK | TABLET | 100 | | 6 |
| 60505-4374-3 | vilazodone hydrochloride | 30 in 1 BOTTLE | TABLET | 30 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60505-4374 | VILAZODONE HYDROCHLORIDE TABLET [APOTEX CORP.] | 6 | Current NDC, 2 package rows | 20250214_a70fd858-cbef-7336-d7ce-c78499031644.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 |
|---|
| 60505-4374-0 | 60505437400 | 100 in 1 BLISTER PACK | | | | | Historical |
| 60505-4374-3 | 60505437403 | 30 TABLET in 1 BOTTLE (60505-4374-3) | 30 tablet | 2023-10-26 | No | No | Historical |