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
31722-691_3241a29b-82b9-fd3a-e063-6294a90aa46c
Product NDC
31722-691
Form
SUSPENSION
Composition / generic term
spironolactone
Labeler
Camber Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20250221
Source listing expiry
20261231

Source-listed ingredients

  • SPIRONOLACTONE — 25 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 118 mL in 1 BOTTLE (31722-691-11) · 31722-691-11
  • 473 mL in 1 BOTTLE (31722-691-47) · 31722-691-47

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.

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