NDC 71610-021
Chlorthalidone 50 mg tablet
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, 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
- Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN, 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
- Feb 12, 2016
- Package NDCs
71610-021-09- Official label
- DailyMed (National Library of Medicine), updated Dec 20, 2017
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?