NDC 63629-1064
Spironolactone 25 mg tablet
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack 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 |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Recalls
- Aug 5, 2025 · Class II · Sun Pharmaceutical Industries Inc
Presence of foreign substance: identified as aluminum.
Lots: Lot # P3314, Exp 11/30/2026 - Jan 27, 2021 · Class I · Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolactone 50 mg tablets.
Lots: a) Lot #: 148969, Exp 7/31/2022, b) Lot #: 148791, Exp 7/31/2022, c) Lot #: 148991, Exp 7/31/2022
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
- Jul 23, 1986
- Package NDCs
63629-1064-163629-1064-263629-1064-363629-1064-463629-1064-563629-1064-6- Official label
- DailyMed (National Library of Medicine), updated Sep 9, 2026
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