NDC 68462-433
colesevelam hydrochloride 625 mg tablet, film coated
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Dhar, India | Makes it and tests it | Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action |
Recalls
- Mar 13, 2025 · Class II · Glenmark Pharmaceuticals Inc., USA
CGMP Deviations
Lots: Lot # 17240669, exp. date Mar-26 17240876, exp. date Apr-26 17240883, exp. date May-26 17240909, exp. date May-26 17240914, exp. date May-26 17240927, exp. date May-26
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Colesevelam: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 625 mg
- Approval
- ANDA ANDA203480
- On the market since
- May 18, 2018
- Package NDCs
68462-433-1868462-433-90- Official label
- DailyMed (National Library of Medicine), updated Jan 29, 2026
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