# Donepezil hydrochloride

NDC: 55111-302
Generic name: Donepezil hydrochloride
Labeler / Manufacturer: Dr. Reddys Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250820

FDA application: ANDA202723

## Active ingredients

- DONEPEZIL HYDROCHLORIDE: 23 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55111-302"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-302
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7c0d3bcb-157d-0414-64ee-055bc614d190