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
- 82804-976_99b119e3-537a-464c-9376-4219bf283753
- Product NDC
- 82804-976
- Form
- TABLET, COATED
- Composition / generic term
- Spironolactone
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210104
- Source listing expiry
- 20261231
Source-listed ingredients
- SPIRONOLACTONE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, COATED in 1 BOTTLE (82804-976-00) · 82804-976-00
- 1000 TABLET, COATED in 1 BOTTLE (82804-976-11) · 82804-976-11
- 30 TABLET, COATED in 1 BOTTLE (82804-976-30) · 82804-976-30
- 500 TABLET, COATED in 1 BOTTLE (82804-976-55) · 82804-976-55
- 60 TABLET, COATED in 1 BOTTLE (82804-976-60) · 82804-976-60
- 120 TABLET, COATED in 1 BOTTLE (82804-976-72) · 82804-976-72
- 90 TABLET, COATED in 1 BOTTLE (82804-976-90) · 82804-976-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →