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Bumetanide

NDC 69238-1490, Bumetanide, tablet, from Amneal Pharmaceuticals NY LLC.

Product NDC
69238-1490
Status
Listed
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209724
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1490 \
  -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
69238-1490-169238149001100 TABLET in 1 BOTTLE (69238-1490-1)
69238-1490-569238149005500 TABLET in 1 BOTTLE (69238-1490-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9188ab17-8539-48a5-905f-ad35ab5a0b93

  • NADAC price for package 69238149001

    GET /v1/drugs/nadac/69238149001

  • NADAC price for package 69238149005

    GET /v1/drugs/nadac/69238149005

Use it

Look up 69238-1490 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1490 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69238-1490. 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.