NDC 0245-0036
Prevalite 4 g per 5.5 g powder, for suspension
On the label: Upsher-Smith Laboratories, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceuticals Inc. | Maple Grove, MN, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections |
Product details
- Generic drug
- Cholestyramine: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 4 g per 5.5 g
- Approval
- ANDA ANDA073263
- On the market since
- Feb 1, 1996
- Package NDCs
0245-0036-230245-0036-420245-0036-600245-0036-89- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2025
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