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SODIUM NITROPRUSSIDE

NDC 42571-265, SODIUM NITROPRUSSIDE, injection, from Micro Labs Limited.

Product NDC
42571-265
Status
Listed
Labeler
Micro Labs Limited
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209352
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42571-265 \
  -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
42571-265-75425710265751 VIAL, SINGLE-DOSE in 1 CARTON (42571-265-75) / 2 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5a599880-c133-44ef-a9f2-bd1b681563be

Use it

Look up 42571-265 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42571-265 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42571-265. 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.