NDC 68462-620
Colesevelam Hydrochloride 3.75 g powder, for suspension
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Goa, India | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Colesevelam: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 3.75 g
- Approval
- ANDA ANDA202190
- On the market since
- Jul 16, 2018
- Package NDCs
68462-620-30- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2026
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