# amantadine hydrochloride

NDC: 68382-512
Generic name: amantadine hydrochloride
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20160804

FDA application: ANDA208278

## 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:"68382-512"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-512
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=609dc911-1e9d-4ebd-b64b-f44054e5582e