NDC 68382-227

amiodarone hydrochloride 200 mg tablet

On the label: Zydus Pharmaceuticals (USA) Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action

Product details

Generic drug
Amiodarone: every company that makes it
Form
tablet, oral
Strength
200 mg
Approval
ANDA ANDA079029
On the market since
Aug 10, 2009
Package NDCs
68382-227-05 68382-227-06 68382-227-10 68382-227-14 68382-227-30 68382-227-77
Official label
DailyMed (National Library of Medicine), updated Mar 16, 2023

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