# Donepezil hydrochloride

NDC: 55111-356
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: 20110531

FDA application: ANDA201001

## 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:"55111-356"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-356
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c9889fd-2cb3-02da-f034-46120acc38c3