# Amantadine Hydrochloride

NDC: 39328-530
Generic name: amantadine hydrochloride
Labeler / Manufacturer: Patrin Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20230811

FDA application: ANDA214178

## Active ingredients

- AMANTADINE HYDROCHLORIDE: 50 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"39328-530"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=39328-530
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0fcf5182-a666-4f38-879f-47f19de30dd5