Vilazodone
- Product NDC
- 60505-4774
- 11-digit product format
- 605054774
- Labeler code
- 60505
- Product ID
- 60505-4774_27cec315-2f77-4048-861e-31e24701b60c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vilazodone hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Apotex Corp
- Application
- NDA022567
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2022-06-04
- Marketing end
- 0000-00-00
- Substance
- VILAZODONE HYDROCHLORIDE
- Active strength
- 40 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60505-4774 | VILAZODONE (VILAZODONE HYDROCHLORIDE) TABLET VILAZODONE (VILAZODONE HYDROCHLORIDE) TABLET [APOTEX CORP] | 4 | Legacy NDC | 20241213_fad37b72-1ebe-4a71-835d-b0c1e4b90011.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-4774-3 | 60505477403 | 30 TABLET in 1 BOTTLE (60505-4774-3) | 30 tablet | 2022-06-04 | 0000-00-00 | No | No | Current |