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
- 76420-925_2fa991e8-8594-6911-e063-6294a90a916d
- Product NDC
- 76420-925
- Form
- TABLET, COATED
- Composition / generic term
- Spironolactone
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210104
- Source listing expiry
- 20261231
Source-listed ingredients
- SPIRONOLACTONE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, COATED in 1 BOTTLE (76420-925-00) · 76420-925-00
- 100 TABLET, COATED in 1 BOTTLE (76420-925-01) · 76420-925-01
- 500 TABLET, COATED in 1 BOTTLE (76420-925-05) · 76420-925-05
- 2500 TABLET, COATED in 1 BOTTLE (76420-925-25) · 76420-925-25
- 30 TABLET, COATED in 1 BOTTLE (76420-925-30) · 76420-925-30
- 60 TABLET, COATED in 1 BOTTLE (76420-925-60) · 76420-925-60
- 90 TABLET, COATED in 1 BOTTLE (76420-925-90) · 76420-925-90
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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