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Bumetanide

NDC 68462-469, Bumetanide, injection, from GLENMARK PHARMACEUTICALS INC., USA.

Product NDC
68462-469
Status
Listed
Labeler
GLENMARK PHARMACEUTICALS INC., USA
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216434
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-469 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUMETANIDE.25 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
68462-469-546846204695410 VIAL, SINGLE-DOSE in 1 CARTON (68462-469-54) / 4 mL in 1 VIAL, SINGLE-DOSE (68462-469-40)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/680563fe-5d3a-49bc-86a5-740bda2acebe

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=68462-469

Use it

Look up 68462-469 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-469 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-469. 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.