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Bumetanide

NDC 70756-081, Bumetanide, tablet, from Lifestar Pharma LLC.

Product NDC
70756-081
Status
Listed
Labeler
Lifestar Pharma 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/70756-081 \
  -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
70756-081-1170756008111100 TABLET in 1 BOTTLE (70756-081-11)
70756-081-5170756008151500 TABLET in 1 BOTTLE (70756-081-51)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/51a344b6-acf9-4ac4-b743-1e63e3df7958

  • NADAC price for package 70756008111

    GET /v1/drugs/nadac/70756008111

  • NADAC price for package 70756008151

    GET /v1/drugs/nadac/70756008151

Use it

Look up 70756-081 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70756-081 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70756-081. 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.