# Donepezil Hydrochloride

NDC: 42658-119
Generic name: Donepezil Hydrochloride
Labeler / Manufacturer: Hisun Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: ORAL
Marketing started: 20250101

FDA application: ANDA205269

## Active ingredients

- DONEPEZIL HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42658-119"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42658-119
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8d682a51-31d0-43e6-9fab-6eb5219f5a41