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epoprostenol

NDC 62756-059, epoprostenol, injection, powder, lyophilized, for solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-059
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210473
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-059 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • EPOPROSTENOL SODIUM.5 mg/10mL

Pharmacologic classes

Prostacycline Vasodilator [EPC]; Prostaglandins I [CS]; Vasodilation [PE]

Package NDCNDC-11Package
62756-059-40627560059401 VIAL in 1 CARTON (62756-059-40) / 10 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/db57e498-db20-45e8-8298-b0cf0811d270

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=62756-059

Use it

Look up 62756-059 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-059 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-059. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.