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Furosemide

NDC 0409-6102, FUROSEMIDE, injection, solution, from Hospira, Inc..

Product NDC
0409-6102
Status
Listed
Labeler
Hospira, Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA018667
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0409-6102 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE10 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
0409-6102-020040961020225 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-02) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-6102-19)
0409-6102-040040961020425 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-04) / 4 mL in 1 VIAL, SINGLE-DOSE (0409-6102-18)
0409-6102-100040961021025 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-10) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-6102-20)
0409-6102-250040961022525 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-25) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-6102-35)
0409-6102-260040961022625 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-26) / 4 mL in 1 VIAL, SINGLE-DOSE (0409-6102-36)
0409-6102-270040961022725 VIAL, SINGLE-DOSE in 1 TRAY (0409-6102-27) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-6102-37)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels?ndc=0409-6102
  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0409-6102
  • NADAC price for package 00409610202

    GET /v1/drugs/nadac/00409610202
  • NADAC price for package 00409610204

    GET /v1/drugs/nadac/00409610204
  • NADAC price for package 00409610225

    GET /v1/drugs/nadac/00409610225
  • NADAC price for package 00409610226

    GET /v1/drugs/nadac/00409610226

Use it

Look up 0409-6102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0409-6102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0409-6102. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.