Skip to content
healthcare.dev

Bumetanide

NDC 70518-4385, Bumetanide, tablet, from REMEDYREPACK INC..

Product NDC
70518-4385
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213942
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4385 \
  -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
70518-4385-07051843850090 TABLET in 1 BOTTLE, PLASTIC (70518-4385-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/de008936-e8a3-4e65-bb6a-d925b68a5f50

Use it

Look up 70518-4385 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4385 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4385. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.