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sodium nitroprusside

NDC 70436-028, sodium nitroprusside, injection, solution, concentrate, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-028
Status
Listed
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214199
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-028 \
  -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
70436-028-80704360028801 VIAL in 1 CARTON (70436-028-80) / 2 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/01dfae56-3d9b-448a-84a7-03a54a533eb1

Use it

Look up 70436-028 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-028 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-028. 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.