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Sodium nitroprusside

NDC 70121-1189, Sodium nitroprusside, injection, from Amneal Pharmaceuticals LLC.

Product NDC
70121-1189
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209493
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70121-1189 \
  -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
70121-1189-1701211189011 VIAL, SINGLE-DOSE in 1 CARTON (70121-1189-1) / 2 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2fa687a2-10e7-45ae-953a-9d63564c2908

Use it

Look up 70121-1189 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70121-1189 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70121-1189. 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.