Trintellix
- Product NDC
- 70518-2642
- 11-digit product format
- 705182642
- Labeler code
- 70518
- Product ID
- 70518-2642_dc760e13-7db8-3808-e053-2a95a90a9327
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vortioxetine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA204447
- Marketing category
- NDA
- Marketing start
- 2020-03-24
- Marketing end
- 0000-00-00
- Substance
- VORTIOXETINE HYDROBROMIDE
- Active strength
- 20 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 |
|---|
| 70518-2642 | TRINTELLIX (VORTIOXETINE) TABLET, FILM COATED [REMEDYREPACK INC.] | 7 | Legacy NDC | 20250418_e572a091-cad9-4ffa-a8eb-28181c0a8222.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2642-0 | 70518264200 | 30 POUCH in 1 BOX (70518-2642-0) > 1 TABLET, FILM COATED in 1 POUCH (70518-2642-1) | 30 pouch | 2020-03-24 | 0000-00-00 | No | No | Current |