Lurasidone Hydrochloride
NDC 13668-465, Lurasidone Hydrochloride, tablet, film coated, from Torrent Pharmaceuticals Limited.
- Product NDC
- 13668-465
- Status
- Listed
- Labeler
- Torrent Pharmaceuticals Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208055
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/13668-465 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LURASIDONE HYDROCHLORIDE40 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 13668-465-30 | 13668046530 | 30 TABLET, FILM COATED in 1 BOTTLE (13668-465-30) |
| 13668-465-90 | 13668046590 | 90 TABLET, FILM COATED in 1 BOTTLE (13668-465-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9cb5e275-1029-407a-8c93-ec5cde2d323bNADAC price for package 13668046530
GET /v1/drugs/nadac/13668046530
Use it
Look up 13668-465 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/13668-465 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 13668-465. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.