# Memantine Hydrochloride

NDC: 61442-192
Generic name: Memantine Hydrochloride
Labeler / Manufacturer: Carlsbad Technology, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250622

FDA application: ANDA212947

## Active ingredients

- MEMANTINE HYDROCHLORIDE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"61442-192"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61442-192
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=30b4d5c4-0a31-c385-e063-6394a90adbce