# Memantine Hydrochloride

NDC: 55154-7637
Generic name: Memantine Hydrochloride
Labeler / Manufacturer: Cardinal Health 107, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20150720

FDA application: ANDA090048

## 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:"55154-7637"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55154-7637
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=65c9e7bc-71f0-4113-8de1-4fcaa591735f