NDC 68071-3969
Spironolactone 25 mg tablet, coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Oxford Pharmaceuticals, LLC's NDC 69584-852.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Oxford Pharmaceuticals, LLC | Birmingham, AL, United States | Makes it | Problems found, fixed voluntarilyNov 3, 2023 · 3 inspections |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Spironolactone: every company that makes it
- Form
- tablet, coated, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA040750
- On the market since
- Jan 4, 2021
- Package NDCs
68071-3969-1- Official label
- DailyMed (National Library of Medicine), updated Feb 25, 2026
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