NALTREXONE HYDROCHLORIDE
NDC 0615-8579, NALTREXONE HYDROCHLORIDE, tablet, film coated, from NCS HealthCare of KY, LLC dba Vangard Labs.
- Product NDC
- 0615-8579
- Status
- Listed
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090356
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8579 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NALTREXONE HYDROCHLORIDE50 mg/1
Pharmacologic classes
Opioid Antagonist [EPC]; Opioid Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0615-8579-39 | 00615857939 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8579-39) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/fa2f842f-001a-4f1e-8748-c7852579109c
Use it
Look up 0615-8579 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8579 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0615-8579. 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.