# donepezil hydrochloride

NDC: 43547-879
Generic name: donepezil hydrochloride
Labeler / Manufacturer: Solco Healthcare US, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20111101

FDA application: ANDA200292

## Active ingredients

- DONEPEZIL HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43547-879"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43547-879
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=48178cb4-4fee-47c0-88e9-a4f017f1f448