# Amiodarone Hydrochloride

NDC: 29300-359
Generic name: Amiodarone Hydrochloride
Labeler / Manufacturer: Unichem Pharmaceuticals (USA), Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200901

FDA application: ANDA213446

## Active ingredients

- AMIODARONE HYDROCHLORIDE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"29300-359"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=29300-359
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a20d0c03-cfda-49d1-88c9-be1bf295bc6c