# Memantine Hydrochloride

NDC: 16571-855
Generic name: memantine
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20250601

FDA application: ANDA206032

## Active ingredients

- MEMANTINE HYDROCHLORIDE: 28 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"16571-855"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-855
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a282fbed-8304-458e-a0e9-5eaccc95339b