BUPRENORPHINE
NDC 42858-501, BUPRENORPHINE, tablet, from Rhodes Pharmaceuticals LLC.
- Product NDC
- 42858-501
- Status
- Listed
- Labeler
- Rhodes Pharmaceuticals LLC
- Dosage form
- TABLET
- Route
- SUBLINGUAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207276
- DEA schedule
- CIII
curl https://api.healthcare.dev/v1/drugs/ndc/42858-501 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUPRENORPHINE HYDROCHLORIDE2 mg/1
Pharmacologic classes
Partial Opioid Agonist [EPC]; Partial Opioid Agonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42858-501-03 | 42858050103 | 30 TABLET in 1 BOTTLE (42858-501-03) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/da90618a-5621-4b15-bc48-9dcc631418deNADAC price for package 42858050103
GET /v1/drugs/nadac/42858050103
Use it
Look up 42858-501 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42858-501 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42858-501. 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.