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Furosemide

NDC 72789-032, furosemide, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-032
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/72789-032 \
  -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
72789-032-307278900323030 TABLET in 1 BOTTLE, PLASTIC (72789-032-30)
72789-032-607278900326060 TABLET in 1 BOTTLE, PLASTIC (72789-032-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/52e75604-5766-40e8-a13a-8c449e06ebda

Use it

Look up 72789-032 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-032 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-032. 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.