# Memantine Hydrochloride

NDC: 33342-298
Generic name: Memantine Hydrochloride
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20151013

FDA application: ANDA202840

## Active ingredients

- MEMANTINE HYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-298"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-298
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=989fa756-7d70-4ea7-bb5e-f4395e48589d