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Bumetanide

NDC 42799-121, Bumetanide, tablet, from Edenbridge Pharmaceuticals LLC..

Product NDC
42799-121
Status
Listed
Labeler
Edenbridge Pharmaceuticals LLC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA018225
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42799-121 \
  -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
42799-121-0142799012101100 TABLET in 1 BOTTLE (42799-121-01)
42799-121-0242799012102500 TABLET in 1 BOTTLE (42799-121-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/32c4372e-54ea-4fc8-b9f8-827fa4c8edd3

  • NADAC price for package 42799012101

    GET /v1/drugs/nadac/42799012101

  • NADAC price for package 42799012102

    GET /v1/drugs/nadac/42799012102

Use it

Look up 42799-121 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42799-121 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42799-121. 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.