NDC 70518-4350
Spironolactone 25 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 53489-143.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Frontida BioPharm, LLC | Philadelphia, PA, United States | Makes it | No problems foundApr 2, 2026 · 10 inspections, 1 with FDA action |
Recalls
- Aug 5, 2025 · Class II · Sun Pharmaceutical Industries Inc
Presence of foreign substance: identified as aluminum.
Lots: Lot # P3314, Exp 11/30/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Spironolactone: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA089424
- On the market since
- May 30, 2025
- Package NDCs
70518-4350-070518-4350-1- Official label
- DailyMed (National Library of Medicine), updated Sep 8, 2026
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