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Furosemide

NDC 63187-739, Furosemide, tablet, from Proficient Rx LP.

Product NDC
63187-739
Status
Listed
Labeler
Proficient Rx LP
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/63187-739 \
  -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
63187-739-106318707391010 TABLET in 1 BOTTLE (63187-739-10)
63187-739-306318707393030 TABLET in 1 BOTTLE (63187-739-30)
63187-739-606318707396060 TABLET in 1 BOTTLE (63187-739-60)
63187-739-906318707399090 TABLET in 1 BOTTLE (63187-739-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/595ddaf2-c2cb-44a4-a46c-53bcfe6bd752

Use it

Look up 63187-739 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63187-739 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63187-739. 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.