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Sodium Nitroprusside

NDC 71288-202, Sodium Nitroprusside, injection, solution, from Meitheal Pharmaceuticals Inc..

Product NDC
71288-202
Status
Listed
Labeler
Meitheal Pharmaceuticals Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211016
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71288-202 \
  -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
71288-202-02712880202021 VIAL, SINGLE-DOSE in 1 CARTON (71288-202-02) / 2 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/820eadcb-1230-4b17-a652-e69b52b3c12f

Use it

Look up 71288-202 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71288-202 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71288-202. 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.