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Furosemide

NDC 43063-716, Furosemide, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-716
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/43063-716 \
  -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
43063-716-0143063071601100 TABLET in 1 BOTTLE, PLASTIC (43063-716-01)
43063-716-304306307163030 TABLET in 1 BOTTLE, PLASTIC (43063-716-30)
43063-716-604306307166060 TABLET in 1 BOTTLE, PLASTIC (43063-716-60)
43063-716-904306307169090 TABLET in 1 BOTTLE, PLASTIC (43063-716-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e20257f6-7cfe-43fa-a672-cc1cb312b83a

Use it

Look up 43063-716 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-716 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-716. 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.