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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
Request
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 NDCNDC-11Package
0781-3158-950078131589510 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-c2dbf79b22eb
  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0781-3158

Use it

Look up 0781-3158 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-3158 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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.