NDC 72789-359
Chlorthalidone 50 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 57664-649.
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
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, 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
- 50 mg
- Approval
- ANDA ANDA089286
- On the market since
- Oct 27, 2023
- Package NDCs
72789-359-3072789-359-90- Official label
- DailyMed (National Library of Medicine), updated Oct 30, 2026
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