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Furosemide

NDC 42291-470, furosemide, tablet, from AvKARE.

Product NDC
42291-470
Status
Listed
Labeler
AvKARE
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076796
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42291-470 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE80 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
42291-470-0142291047001100 TABLET in 1 BOTTLE (42291-470-01)
42291-470-5042291047050500 TABLET in 1 BOTTLE (42291-470-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d4c532be-1f3f-60d3-e053-2995a90a98be

Use it

Look up 42291-470 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42291-470 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42291-470. 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.