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SODIUM NITROPRUSSIDE

NDC 55150-320, SODIUM NITROPRUSSIDE, injection, from AuroMedics Pharma LLC.

Product NDC
55150-320
Status
Listed
Labeler
AuroMedics Pharma LLC
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211934
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55150-320 \
  -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
55150-320-01551500320011 VIAL, SINGLE-DOSE in 1 CARTON (55150-320-01) / 2 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/41e11afb-5fa4-4212-889d-1092dbd0702a

Use it

Look up 55150-320 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55150-320 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55150-320. 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.