Class II · Moderate risk
Donepezil HCl Tablets
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
National Drug Code
Is NDC 43547-0276-09 recalled?
donepezil hydrochloride · 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-09)
Yes — this exact package was recalled
1 FDA recall names the code 43547-0276-09 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- donepezil hydrochloride
- Strength
- DONEPEZIL HYDROCHLORIDE 10 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Solco Healthcare US, LLC
- Type
- Human Prescription Drug
- Product code
- 43547-0276
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 43547-0331 Irbesartan and Hydrochlorothiazide 3
- 43547-0369 Valsartan 3
- 43547-0330 Irbesartan and Hydrochlorothiazide 2
- 43547-0275 donepezil hydrochloride 1
- 43547-0311 Valsartan and Hydrochlorothiazide 1
- 43547-0312 Valsartan and Hydrochlorothiazide 1
Free recall alerts
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