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bumetanide

NDC 23155-900, bumetanide, tablet, from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..

Product NDC
23155-900
Status
Listed
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
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/23155-900 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUMETANIDE.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
23155-900-0123155090001100 TABLET in 1 BOTTLE (23155-900-01)
23155-900-0523155090005500 TABLET in 1 BOTTLE (23155-900-05)
23155-900-10231550900101000 TABLET in 1 BOTTLE (23155-900-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d4688d53-9baf-4cf0-b37f-47779bce7815

Use it

Look up 23155-900 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/23155-900 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 23155-900. 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.