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bumetanide

NDC 68382-525, bumetanide, tablet, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
68382-525
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202900
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-525 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUMETANIDE.5 mg/1

Pharmacologic classes

Increased Diuresis at Loop of Henle [PE]; Loop Diuretic [EPC]

Package NDCNDC-11Package
68382-525-0168382052501100 TABLET in 1 BOTTLE (68382-525-01)
68382-525-0568382052505500 TABLET in 1 BOTTLE (68382-525-05)
68382-525-066838205250630 TABLET in 1 BOTTLE (68382-525-06)
68382-525-10683820525101000 TABLET in 1 BOTTLE (68382-525-10)
68382-525-166838205251690 TABLET in 1 BOTTLE (68382-525-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/525138cd-832a-41d0-84b0-83921b12bd2a

Use it

Look up 68382-525 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-525 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-525. 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.