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Furosemide

NDC 42571-436, Furosemide, injection, from Micro Labs Limited.

Product NDC
42571-436
Status
Listed
Labeler
Micro Labs Limited
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218188
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42571-436 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE20 mg/2mL

Pharmacologic classes

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

Package NDCNDC-11Package
42571-436-874257104368725 VIAL in 1 CARTON (42571-436-87) / 2 mL in 1 VIAL (42571-436-75)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2f547f7c-0322-465c-9764-43f955d98ab2

Use it

Look up 42571-436 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42571-436 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42571-436. 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.