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Furosemide

NDC 0054-4301, Furosemide, tablet, from Hikma Pharmaceuticals USA Inc..

Product NDC
0054-4301
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA070086
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0054-4301 \
  -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
0054-4301-2500054430125100 TABLET in 1 BOTTLE, PLASTIC (0054-4301-25)
0054-4301-2900054430129500 TABLET in 1 BOTTLE, PLASTIC (0054-4301-29)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9e493331-dddd-496e-abf8-61747fb67aba
  • NADAC price for package 00054430125

    GET /v1/drugs/nadac/00054430125
  • NADAC price for package 00054430129

    GET /v1/drugs/nadac/00054430129

Use it

Look up 0054-4301 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0054-4301 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0054-4301. 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.