bivalirudin
NDC 0781-3158, bivalirudin, injection, powder, lyophilized, for solution, from Sandoz Inc.
- Product NDC
- 0781-3158
- Status
- Listed
- Labeler
- Sandoz Inc
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA020873
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0781-3158 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BIVALIRUDIN250 mg/1
Pharmacologic classes
Anti-coagulant [EPC]; Direct Thrombin Inhibitor [EPC]; Thrombin Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0781-3158-95 | 00781315895 | 10 VIAL, SINGLE-USE in 1 CARTON (0781-3158-95) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE (0781-3158-94) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/ce56f806-7845-429d-a1ce-c2dbf79b22ebMedicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=0781-3158
Use it
Look up 0781-3158 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0781-3158 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0781-3158. 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.