# Memantine hydrochloride

NDC: 33342-220
Generic name: Memantine hydrochloride
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250828

FDA application: ANDA206310

## Active ingredients

- MEMANTINE HYDROCHLORIDE: 14 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-220"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-220
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=62e32b0b-1eb2-424d-bfd2-d27ef27d35f3