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
- 63629-4094_0e68cdd6-df1b-40f6-84a0-7a7d48b6cf23
- Product NDC
- 63629-4094
- 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 — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (63629-4094-1) · 63629-4094-1
- 3 TABLET, FILM COATED in 1 BOTTLE (63629-4094-2) · 63629-4094-2
- 30 TABLET, FILM COATED in 1 BOTTLE (63629-4094-3) · 63629-4094-3
- 90 TABLET, FILM COATED in 1 BOTTLE (63629-4094-4) · 63629-4094-4
- 60 TABLET, FILM COATED in 1 BOTTLE (63629-4094-5) · 63629-4094-5
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 →