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
- 63629-1830_e2c30b41-efb4-4443-8a4b-d6bbfc2132a1
- Product NDC
- 63629-1830
- Form
- TABLET
- Composition / generic term
- SPIRONOLACTONE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19860723 / 20290228
Source-listed ingredients
- SPIRONOLACTONE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (63629-1830-1) · 63629-1830-1
- 60 TABLET in 1 BOTTLE (63629-1830-2) · 63629-1830-2
- 90 TABLET in 1 BOTTLE (63629-1830-3) · 63629-1830-3
- 14 TABLET in 1 BOTTLE (63629-1830-4) · 63629-1830-4
- 100 TABLET in 1 BOTTLE (63629-1830-5) · 63629-1830-5
- 7 TABLET in 1 BOTTLE (63629-1830-6) · 63629-1830-6
- 10 TABLET in 1 BOTTLE (63629-1830-7) · 63629-1830-7
- 180 TABLET in 1 BOTTLE (63629-1830-8) · 63629-1830-8
- 45 TABLET in 1 BOTTLE (63629-1830-9) · 63629-1830-9
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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