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Furosemide

NDC 69315-118, Furosemide, tablet, from Leading Pharma, LLC.

Product NDC
69315-118
Status
Listed
Labeler
Leading Pharma, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077293
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69315-118 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE80 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
69315-118-0169315011801100 TABLET in 1 BOTTLE (69315-118-01)
69315-118-0569315011805500 TABLET in 1 BOTTLE (69315-118-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b5c6fcf4-fd37-4fee-8dac-1a3273d95ffe

  • NADAC price for package 69315011801

    GET /v1/drugs/nadac/69315011801

  • NADAC price for package 69315011805

    GET /v1/drugs/nadac/69315011805

Use it

Look up 69315-118 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69315-118 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69315-118. 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.