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Furosemide

NDC 73542-101, Furosemide, injection, from Maiva Pharma Private Limited.

Product NDC
73542-101
Status
Listed
Labeler
Maiva Pharma Private Limited
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203428
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73542-101 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE10 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
73542-101-257354201012525 VIAL in 1 CARTON (73542-101-25) / 2 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e5880bf4-5037-4813-b7cc-656a6832ecb5

Use it

Look up 73542-101 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73542-101 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73542-101. 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.