United States · FDA National Drug Code directory

Ethacrynic Acid

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
50228-334_2a0ab1c4-a5f5-aeed-e063-6394a90a5992
Product NDC
50228-334
Form
TABLET
Composition / generic term
Ethacrynic Acid
Labeler
ScieGen Pharmaceuticals Inc
Marketing category
ANDA
Marketing start / end (source format)
20190827
Source listing expiry
20261231

Source-listed ingredients

  • ETHACRYNIC ACID — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET in 1 BOTTLE (50228-334-01) · 50228-334-01
  • 100 TABLET in 1 BOTTLE (50228-334-10) · 50228-334-10
  • 30 TABLET in 1 BOTTLE (50228-334-30) · 50228-334-30

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 →