# Memantine Hydrochloride

NDC: 69680-162
Generic name: memantine hydrochloride
Labeler / Manufacturer: Vitruvias Therapeutics, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20231215

FDA application: ANDA213985

## 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:"69680-162"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69680-162
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0c7fd6ab-2ce5-4110-b6e6-9103c8da0765