# Memantine hydrochloride

NDC: 53746-169
Generic name: Memantine
Labeler / Manufacturer: Amneal Pharmaceuticals of New York LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20150430

FDA application: ANDA090041

## Active ingredients

- MEMANTINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"53746-169"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53746-169
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=054069b5-7aac-4106-821f-ebf7fd531b4f