# Memantine Hydrochloride

NDC: 0832-1112
Generic name: Memantine Hydrochloride
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20150731
Marketing ended: 20280131
FDA application: ANDA090043

## 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:"0832-1112"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0832-1112
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6e0ade9e-b721-4701-bcb7-de464e19e707