# Memantine

NDC: 60687-173
Generic name: Memantine
Labeler / Manufacturer: American Health Packaging
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150803

FDA application: ANDA090048

## 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:"60687-173"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60687-173
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=304a3059-4f7f-4ec4-839d-86492bb5e07b