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FUROSEMIDE

NDC 51662-1720, FUROSEMIDE, injection, solution, from HF Acquisition Co LLC, DBA HealthFirst.

Product NDC
51662-1720
Status
Listed
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217557
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1720 \
  -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
51662-1720-35166217200325 POUCH in 1 BOX (51662-1720-3) / 1 VIAL, GLASS in 1 POUCH (51662-1720-2) / 10 mL in 1 VIAL, GLASS (51662-1720-1)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5e37f97b-f5db-23a0-e063-6394a90a9b72

Use it

Look up 51662-1720 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1720 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51662-1720. 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.