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Bumetanide

NDC 72603-900, Bumetanide, tablet, from NorthStar Rx LLC.

Product NDC
72603-900
Status
Listed
Labeler
NorthStar Rx LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213942
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72603-900 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUMETANIDE1 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72603-900-0172603090001100 TABLET in 1 BOTTLE (72603-900-01)
72603-900-0272603090002500 TABLET in 1 BOTTLE (72603-900-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/551918e1-96c4-453a-870c-61b282882206

  • NADAC price for package 72603090001

    GET /v1/drugs/nadac/72603090001

Use it

Look up 72603-900 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72603-900 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72603-900. 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.