NDC 60687-317
Chlorthalidone 25 mg tablet
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 57664-648.
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
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Feb 7, 2022 · Class II · Sun Pharmaceutical Industries Inc
Foreign Matter identified as stainless steel microscopic wear particles mixed with punch lubricant oil and silicone particles from the dust cup
Lots: Lot #: P0602, Exp. Date 03/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Chlorthalidone: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA089286
- On the market since
- Aug 10, 2017
- Package NDCs
60687-317-0160687-317-1160687-317-2560687-317-95- Official label
- DailyMed (National Library of Medicine), updated Nov 13, 2025
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