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Sodium Nitroprusside

NDC 71839-120, Sodium Nitroprusside, injection, from BE Pharmaceuticals Inc..

Product NDC
71839-120
Status
Listed
Labeler
BE Pharmaceuticals Inc.
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214971
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71839-120 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM NITROPRUSSIDE50 mg/2mL

Pharmacologic classes

Vasodilation [PE]; Vasodilator [EPC]

Package NDCNDC-11Package
71839-120-01718390120011 VIAL in 1 CARTON (71839-120-01) / 2 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/01841345-bed3-458f-8e99-911fbd286512

Use it

Look up 71839-120 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71839-120 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71839-120. 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.