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
- 17856-1233_5a203aec-a8c0-ffc7-e063-6394a90aba88
- Product NDC
- 17856-1233
- Form
- SUSPENSION
- Composition / generic term
- spironolactone
- Labeler
- Atlantic Biologicals Corp.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20231031
- Source listing expiry
- 20271231
Source-listed ingredients
- SPIRONOLACTONE — 25 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 110 SYRINGE in 1 CASE (17856-1233-1) / 1 mL in 1 SYRINGE · 17856-1233-1
- 45 SYRINGE in 1 CASE (17856-1233-2) / 2.5 mL in 1 SYRINGE · 17856-1233-2
- 110 SYRINGE in 1 CASE (17856-1233-3) / 3 mL in 1 SYRINGE · 17856-1233-3
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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