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
- 50090-0136_cf9f980d-eb9a-41ea-b7f1-bbe03a408037
- Product NDC
- 50090-0136
- Form
- TABLET
- Composition / generic term
- SPIRONOLACTONE
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19860723
- Source listing expiry
- 20261231
Source-listed ingredients
- SPIRONOLACTONE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (50090-0136-0) · 50090-0136-0
- 30 TABLET in 1 BOTTLE, PLASTIC (50090-0136-1) · 50090-0136-1
- 90 TABLET in 1 BOTTLE, PLASTIC (50090-0136-6) · 50090-0136-6
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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