Buprenorphine
NDC 62756-459, Buprenorphine, tablet, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 62756-459
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- TABLET
- Route
- SUBLINGUAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA201760
- DEA schedule
- CIII
curl https://api.healthcare.dev/v1/drugs/ndc/62756-459 \ -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 |
|---|---|---|
| 62756-459-64 | 62756045964 | 3 BLISTER PACK in 1 CARTON (62756-459-64) / 10 TABLET in 1 BLISTER PACK |
| 62756-459-83 | 62756045983 | 30 TABLET in 1 BOTTLE (62756-459-83) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9fd1f18f-0b0f-4059-b603-19ecbf0ed63aNADAC price for package 62756045983
GET /v1/drugs/nadac/62756045983
Use it
Look up 62756-459 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/62756-459 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 62756-459. 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.