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Furosemide

NDC 62135-753, Furosemide, tablet, from Chartwell RX, LLC.

Product NDC
62135-753
Status
Listed
Labeler
Chartwell RX, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA018413
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62135-753 \
  -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
62135-753-906213507539090 TABLET in 1 PACKAGE (62135-753-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8ebd2f10-acfc-48a4-a5db-f20377bda9ce

  • NADAC price for package 62135075390

    GET /v1/drugs/nadac/62135075390

Use it

Look up 62135-753 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62135-753 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62135-753. 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.