TRYNGOLZA
NDC 71860-101, olezarsen sodium, injection, solution, from Ionis Pharmaceuticals, Inc..
- Product NDC
- 71860-101
- Status
- Listed
- Labeler
- Ionis Pharmaceuticals, Inc.
- Dosage form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA218614
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71860-101 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- OLEZARSEN SODIUM80 mg/.8mL
Pharmacologic classes
APOC-III-directed RNA Interaction [EPC]; Antisense Oligonucleotide [EPC]; Antisense [CS]; Increased RNA Degradation [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71860-101-01 | 71860010101 | 1 SYRINGE, GLASS in 1 CARTON (71860-101-01) / .8 mL in 1 SYRINGE, GLASS |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/0f51aa8e-8475-8cf9-e063-6394a90a6848
Use it
Look up 71860-101 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71860-101 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71860-101. 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.