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Furosemide

NDC 17224-185, FUROSEMIDE, tablet, from Calvin Scott & Co., Inc..

Product NDC
17224-185
Status
Listed
Labeler
Calvin Scott & Co., Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077293
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17224-185 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
17224-185-211722401852121 TABLET in 1 BOTTLE, PLASTIC (17224-185-21)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b2cc89e5-6619-4113-ad31-48076652c856

Use it

Look up 17224-185 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17224-185 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17224-185. 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.