NDC 67046-144
donepezil hydrochloride 10 mg tablet, film coated
On the label: Coupler Enterprises Inc.. It's repackaged: Coupler Enterprises Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-276.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Solco Healthcare U.S., LLC names for other drugs.
Repackaging site
- Coupler Enterprises, Location not on file · repackages it
Recalls
- Jan 26, 2022 · Class II · Cardinal Healthcare
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Lots: Batch 17616 - Jan 26, 2022 · Class II · Cardinal Healthcare
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Lots: Batch 17605
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Donepezil: every company that makes it
- Form
- tablet, film coated
- Strength
- 10 mg
- Approval
- ANDA ANDA200292
- On the market since
- Sep 19, 2017
- Package NDCs
67046-144-0767046-144-1467046-144-1567046-144-2167046-144-2867046-144-30- Official label
- DailyMed (National Library of Medicine), updated Dec 19, 2018
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