# Donepezil

NDC: 31722-737
Generic name: Donepezil hydrochloride
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150202

FDA application: ANDA203034

## 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:"31722-737"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-737
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=11ac01f4-d26e-47b2-9660-d514ab097fdb