LAZCLUZE
NDC 57894-080, lazertinib, tablet, film coated, from Janssen Biotech, Inc..
- Product NDC
- 57894-080
- Status
- Listed
- Labeler
- Janssen Biotech, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA219008
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/57894-080 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LAZERTINIB80 mg/1
Pharmacologic classes
Breast Cancer Resistance Protein Inhibitors [MoA]; Cytochrome P450 3A4 Inhibitors [MoA]; Kinase Inhibitor [EPC]; Kinase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 57894-080-60 | 57894008060 | 1 BOTTLE in 1 CARTON (57894-080-60) / 60 TABLET, FILM COATED in 1 BOTTLE |
| 57894-080-90 | 57894008090 | 1 BOTTLE in 1 CARTON (57894-080-90) / 90 TABLET, FILM COATED in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c417f9ee-2027-4ed5-92ad-3c19266de16c
Use it
Look up 57894-080 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/57894-080 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 57894-080. 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.