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Furosemide

NDC 17856-3294, Furosemide, solution, from Atlantic Biologicals Corp..

Product NDC
17856-3294
Status
Listed
Labeler
Atlantic Biologicals Corp.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA070434
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-3294 \
  -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
17856-3294-117856329401120 SYRINGE in 1 CASE (17856-3294-1) / 3 mL in 1 SYRINGE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/54ed0dd9-2fa8-269a-e063-6294a90a607c

Use it

Look up 17856-3294 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-3294 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-3294. 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.