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Furosemide

NDC 68071-4522, furosemide, tablet, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-4522
Status
Listed
Labeler
NuCare 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/68071-4522 \
  -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
68071-4522-168071452201100 TABLET in 1 BOTTLE (68071-4522-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7316929d-413a-e78f-e053-2a91aa0a417e

Use it

Look up 68071-4522 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-4522 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-4522. 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.