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sodium nitroprusside in 0.9% sodium chloride

NDC 70436-205, sodium nitroprusside in 0.9% sodium chloride, injection, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-205
Status
Listed
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215846
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-205 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM NITROPRUSSIDE.2 mg/mL

Pharmacologic classes

Vasodilation [PE]; Vasodilator [EPC]

Package NDCNDC-11Package
70436-205-80704360205801 VIAL, SINGLE-DOSE in 1 CARTON (70436-205-80) / 50 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6f02e4ac-5f7c-4003-b9b7-283f489cddb0

Use it

Look up 70436-205 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-205 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-205. 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.