# memantine hydrochloride

NDC: 65162-169
Generic name: memantine
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220324

FDA application: ANDA090041

## Active ingredients

- MEMANTINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65162-169"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-169
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f73e0df0-4af4-42f1-bde6-3cccb47ca378