# DONEPEZIL HYDROCHLORIDE

NDC: 71209-019
Generic name: donepezil hydrochloride
Labeler / Manufacturer: Cadila Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170130

FDA application: ANDA204609

## Active ingredients

- DONEPEZIL HYDROCHLORIDE: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71209-019"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71209-019
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=37aa1285-774a-4714-a4af-4e3fa9fa7f55