# Donepezil hydrochloride

NDC: 42799-954
Generic name: Donepezil hydrochloride
Labeler / Manufacturer: Edenbridge Pharmaceuticals LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160219

FDA application: ANDA203713

## 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:"42799-954"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42799-954
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=11404dc3-1bde-4d4e-8386-006b67ee19dd