# Memantine hydrochloride

NDC: 52605-072
Generic name: Memantine hydrochloride
Labeler / Manufacturer: POLYGEN PHARMACEUTICALS INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210701

FDA application: ANDA210587

## 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:"52605-072"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52605-072
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c343b0c5-3bfc-4b94-9483-a56924f6dcdb