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Furosemide

NDC 43063-702, Furosemide, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-702
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/43063-702 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FUROSEMIDE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
43063-702-214306307022121 TABLET in 1 BOTTLE, PLASTIC (43063-702-21)
43063-702-304306307023030 TABLET in 1 BOTTLE, PLASTIC (43063-702-30)
43063-702-604306307026060 TABLET in 1 BOTTLE, PLASTIC (43063-702-60)
43063-702-79430630702791 TABLET in 1 BOTTLE, PLASTIC (43063-702-79)
43063-702-904306307029090 TABLET in 1 BOTTLE, PLASTIC (43063-702-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7842eeab-decf-47e7-9134-0add90549a3d

Use it

Look up 43063-702 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-702 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-702. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.