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Bumex

NDC 30698-631, Bumetanide, tablet, from Validus Pharmaceuticals LLC.

Product NDC
30698-631
Status
Listed
Labeler
Validus Pharmaceuticals LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA018225
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/30698-631 \
  -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
30698-631-0130698063101100 TABLET in 1 BOTTLE (30698-631-01)
30698-631-0530698063105500 TABLET in 1 BOTTLE (30698-631-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/32dfbea3-eb2b-4070-8605-57ce3e6d5a2f

Use it

Look up 30698-631 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/30698-631 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 30698-631. 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.