# Amiodarone hydrochloride

NDC: 65841-631
Generic name: Amiodarone hydrochloride
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20090810

FDA application: ANDA079029

## Active ingredients

- AMIODARONE HYDROCHLORIDE: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65841-631"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65841-631
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e8db251-e3c5-4fba-be9a-6044a92f0beb