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Furosemide

NDC 43063-849, furosemide, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-849
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/43063-849 \
  -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
43063-849-214306308492121 TABLET in 1 BOTTLE, PLASTIC (43063-849-21)
43063-849-304306308493030 TABLET in 1 BOTTLE, PLASTIC (43063-849-30)
43063-849-604306308496060 TABLET in 1 BOTTLE, PLASTIC (43063-849-60)
43063-849-904306308499090 TABLET in 1 BOTTLE, PLASTIC (43063-849-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3ba730ab-90d4-478a-80b3-1ea3edb03e4d

Use it

Look up 43063-849 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-849 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-849. 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.