# Donepezil Hydrochloride

NDC: 16571-779
Generic name: Donepezil Hydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20110531

FDA application: ANDA090056

## 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:"16571-779"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-779
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=86b0c5a0-ff3c-4840-a4ac-82af922d58bf