# Memantine hydrochloride

NDC: 68382-549
Generic name: Memantine hydrochloride
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20180408

FDA application: ANDA203293

## 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:"68382-549"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-549
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eac265e6-6ea4-4368-acff-2efe6a8dd40a