# Memantine and Donepezil

NDC: 33342-313
Generic name: Memantine and Donepezil
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250715

FDA application: ANDA208672

## Active ingredients

- DONEPEZIL HYDROCHLORIDE: 10 mg/1
- MEMANTINE HYDROCHLORIDE: 28 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-313"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-313
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3d9a23dc-8cbe-47c3-a048-70d86cb9dc14