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Bumetanide

NDC 51672-4225, Bumetanide, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4225
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213458
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4225 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUMETANIDE2 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51672-4225-151672422501100 TABLET in 1 BOTTLE (51672-4225-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5c753aae-77b7-4add-8453-385a8f62d7db

  • NADAC price for package 51672422501

    GET /v1/drugs/nadac/51672422501

Use it

Look up 51672-4225 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4225 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4225. 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.