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
- 72189-496_2c4e3f99-d912-b742-e063-6294a90a5d1d
- Product NDC
- 72189-496
- Form
- TABLET, COATED
- Composition / generic term
- Spironolactone
- Labeler
- Direct_Rx
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230706
- Source listing expiry
- 20261231
Source-listed ingredients
- SPIRONOLACTONE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, COATED in 1 BOTTLE (72189-496-30) · 72189-496-30
- 90 TABLET, COATED in 1 BOTTLE (72189-496-90) · 72189-496-90
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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