# Amantadine Hydrochloride

NDC: 0832-0111
Generic name: amantadine hydrochloride
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20111215
Marketing ended: 20280229
FDA application: ANDA076186

## 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:"0832-0111"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0832-0111
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=63d9d4aa-5f92-45b0-98d0-d6ec38b727cb