United States · FDA National Drug Code directory

Furosemide

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
62135-753_31443d9b-3dee-5aa9-e063-6294a90adcfd
Product NDC
62135-753
Form
TABLET
Composition / generic term
Furosemide
Labeler
Chartwell RX, LLC
Marketing category
NDA AUTHORIZED GENERIC
Marketing start / end (source format)
19831130
Source listing expiry
20261231

Source-listed ingredients

  • FUROSEMIDE — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET in 1 PACKAGE (62135-753-90) · 62135-753-90

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →