United States · FDA National Drug Code directory
Spironolactone
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
- 76420-062_06c94882-1323-c834-e063-6394a90a2d75
- Product NDC
- 76420-062
- Form
- TABLET, FILM COATED
- Composition / generic term
- spironolactone
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170602
- Source listing expiry
- 20261231
Source-listed ingredients
- SPIRONOLACTONE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (76420-062-01) · 76420-062-01
- 30 TABLET, FILM COATED in 1 BOTTLE (76420-062-30) · 76420-062-30
- 60 TABLET, FILM COATED in 1 BOTTLE (76420-062-60) · 76420-062-60
- 90 TABLET, FILM COATED in 1 BOTTLE (76420-062-90) · 76420-062-90
Source and coverage
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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.
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