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Furosemide

NDC 72162-1361, furosemide, tablet, from Bryant Ranch Prepack.

Product NDC
72162-1361
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076796
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1361 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72162-1361-0721621361001000 TABLET in 1 BOTTLE, PLASTIC (72162-1361-0)
72162-1361-172162136101100 TABLET in 1 BOTTLE, PLASTIC (72162-1361-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/020bc039-9e99-4895-96f8-0c6a556d3e67

Use it

Look up 72162-1361 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1361 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1361. 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.