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Furosemide

NDC 17856-3298, Furosemide, solution, from Atlantic Biologicals Corps.

Product NDC
17856-3298
Status
Listed
Labeler
Atlantic Biologicals Corps
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA070433
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-3298 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE40 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
17856-3298-1178563298015 mL in 1 CUP (17856-3298-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9c342198-7162-4cc5-bda1-bc4054a4292b

Use it

Look up 17856-3298 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-3298 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-3298. 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.