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bumetanide

NDC 72603-299, bumetanide, tablet, from NorthStar Rx, LLC.

Product NDC
72603-299
Status
Listed
Labeler
NorthStar Rx, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074225
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72603-299 \
  -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
72603-299-0172603029901100 TABLET in 1 BOTTLE (72603-299-01)
72603-299-0272603029902500 TABLET in 1 BOTTLE (72603-299-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6b92460e-48ba-44bb-9b61-5e65e5fd82cd

Use it

Look up 72603-299 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72603-299 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72603-299. 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.