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Furosemide

NDC 70518-3757, Furosemide, tablet, from REMEDYREPACK INC..

Product NDC
70518-3757
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216629
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3757 \
  -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
70518-3757-07051837570030 TABLET in 1 BLISTER PACK (70518-3757-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dba00759-87b4-4ecf-998e-ba03ed3d2f1a

Use it

Look up 70518-3757 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3757 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3757. 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.