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
- 72162-1626_bfe78069-1785-4ba7-a2f6-71e8966976c7
- Product NDC
- 72162-1626
- Form
- TABLET, FILM COATED
- Composition / generic term
- SPIRONOLACTONE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19860723
- Source listing expiry
- 20271231
Source-listed ingredients
- SPIRONOLACTONE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (72162-1626-1) · 72162-1626-1
- 30 TABLET, FILM COATED in 1 BOTTLE (72162-1626-3) · 72162-1626-3
- 500 TABLET, FILM COATED in 1 BOTTLE (72162-1626-5) · 72162-1626-5
- 60 TABLET, FILM COATED in 1 BOTTLE (72162-1626-6) · 72162-1626-6
- 90 TABLET, FILM COATED in 1 BOTTLE (72162-1626-9) · 72162-1626-9
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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