Buprenorphine HCl
NDC 31722-870, Buprenorphine HCl, tablet, from Camber Pharmaceuticals, Inc..
- Product NDC
- 31722-870
- Status
- Listed
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- SUBLINGUAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA219401
- DEA schedule
- CIII
curl https://api.healthcare.dev/v1/drugs/ndc/31722-870 \ -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 |
|---|---|---|
| 31722-870-30 | 31722087030 | 30 TABLET in 1 BOTTLE (31722-870-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b52cea0e-688f-4beb-bf7d-f228b81dbd23NADAC price for package 31722087030
GET /v1/drugs/nadac/31722087030
Use it
Look up 31722-870 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/31722-870 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 31722-870. 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.