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Bumetanide

NDC 0781-8160, Bumetanide, tablet, from Sandoz Inc.

Product NDC
0781-8160
Status
Listed
Labeler
Sandoz Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074700
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-8160 \
  -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
0781-8160-0100781816001100 TABLET in 1 BOTTLE (0781-8160-01)
0781-8160-0500781816005500 TABLET in 1 BOTTLE (0781-8160-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8914d8bf-61b7-4cd2-a8ef-7e1c5df37828

Use it

Look up 0781-8160 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-8160 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-8160. 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.