# Amantadine Hydrochloride

NDC: 0591-4920
Generic name: Amantadine Hydrochloride
Labeler / Manufacturer: Actavis Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170103
Marketing ended: 20260630
FDA application: ANDA208096

## Active ingredients

- AMANTADINE HYDROCHLORIDE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0591-4920"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0591-4920
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d9c9eaf7-dcc7-49c1-99d4-49f4dac3779f