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Bumetanide

NDC 81469-222, Bumetanide, tablet, from First Nation Group, LLC.

Product NDC
81469-222
Status
Listed
Labeler
First Nation Group, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219291
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/81469-222 \
  -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
81469-222-0181469022201100 TABLET in 1 BOTTLE (81469-222-01)
81469-222-0581469022205500 TABLET in 1 BOTTLE (81469-222-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/79b77945-74a7-4cb5-8aa0-33a7babdf6d9

Use it

Look up 81469-222 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/81469-222 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 81469-222. 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.