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FUROSCIX

NDC 71767-100, furosemide injection 80 mg/ 10 mL, injection, from scPharmaceuticals Inc., a wholly owned subsidiary of MannKind Corporation.

Product NDC
71767-100
Status
Listed
Labeler
scPharmaceuticals Inc., a wholly owned subsidiary of MannKind Corporation
Dosage form
INJECTION
Route
SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA209988
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71767-100 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE8 mg/mL

Pharmacologic classes

Increased Diuresis at Loop of Henle [PE]; Loop Diuretic [EPC]

Package NDCNDC-11Package
71767-100-01717670100011 CARTON in 1 KIT (71767-100-01) / 1 CARTRIDGE in 1 CARTON / 10 mL in 1 CARTRIDGE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/eac958dd-8d43-e44e-e053-2995a90a4d5e

Use it

Look up 71767-100 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71767-100 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71767-100. 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.