lurasidone hydrochloride
NDC 16729-346, lurasidone hydrochloride, tablet, film coated, from Accord Healthcare, Inc..
- Product NDC
- 16729-346
- Status
- Listed
- Labeler
- Accord Healthcare, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208049
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/16729-346 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LURASIDONE HYDROCHLORIDE20 mg/1
Pharmacologic classes
Atypical Antipsychotic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 16729-346-10 | 16729034610 | 30 TABLET, FILM COATED in 1 BOTTLE (16729-346-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/7e11ec22-63c1-41a6-899c-4fe746f76bd0
Use it
Look up 16729-346 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/16729-346 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 16729-346. 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.