# Memantine and Donepezil Hydrochlorides Extended-release

NDC: 69238-1248
Generic name: Memantine and Donepezil
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20170201

FDA application: ANDA208328

## Active ingredients

- DONEPEZIL HYDROCHLORIDE: 10 mg/1
- MEMANTINE HYDROCHLORIDE: 14 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69238-1248"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69238-1248
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2335950c-be3b-4248-ad04-e9763aee47d2