NDC 65862-325
Donepezil Hydrochloride 5 mg tablet, film coated
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
| Aurolife Pharma LLC | Dayton, NJ, United States | Makes it | Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action |
Product details
- Generic drug
- Donepezil: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA090056
- On the market since
- May 31, 2011
- Package NDCs
65862-325-0165862-325-0565862-325-1065862-325-3065862-325-9065862-325-99- Official label
- DailyMed (National Library of Medicine), updated Jan 8, 2024
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