# Amantadine Hydrochloride

NDC: 16571-834
Generic name: Amantadine Hydrochloride
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20220905

FDA application: ANDA210129

## 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:"16571-834"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-834
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6fd54e00-a714-4442-af95-2515ab3b2ac3