# Memantine Hydrochloride

NDC: 71610-885
Generic name: Memantine Hydrochloride
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150827

FDA application: ANDA206528

## 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:"71610-885"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-885
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=30b8b982-db74-7cf4-e063-6394a90a3a6b