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Sodium Nitroprusside

NDC 70069-261, Sodium Nitroprusside, injection, solution, concentrate, from Somerset Therapeutics, LLC.

Product NDC
70069-261
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210882
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-261 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SODIUM NITROPRUSSIDE25 mg/mL

Pharmacologic classes

Vasodilation [PE]; Vasodilator [EPC]

Package NDCNDC-11Package
70069-261-01700690261011 VIAL in 1 CARTON (70069-261-01) / 2 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2122b9c1-0af4-493b-82cc-63eee02f987f

Use it

Look up 70069-261 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-261 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-261. 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.