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Bumetanide

NDC 65219-570, Bumetanide, injection, from Fresenius Kabi USA, LLC.

Product NDC
65219-570
Status
Listed
Labeler
Fresenius Kabi USA, LLC
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/65219-570 \
  -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
65219-570-046521905700410 VIAL, SINGLE-DOSE in 1 CARTON (65219-570-04) / 4 mL in 1 VIAL, SINGLE-DOSE (65219-570-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a007f3aa-3977-4be3-a9a2-db3d458bca58

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=65219-570

Use it

Look up 65219-570 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65219-570 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65219-570. 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.