# memantine hydrochloride

NDC: 0904-6735
Generic name: memantine hydrochloride
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20180220

FDA application: ANDA206028

## 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:"0904-6735"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-6735
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6ce7cca-d245-44f2-986c-2a8d85dbb5fb