NDC 51862-241

Amiodarone Hydrochloride 200 mg tablet

On the label: Mayne Pharma Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Catalent Greenville, Inc.Greenville, NC, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyOct 24, 2025 · 13 inspections

Product details

Generic drug
Amiodarone: every company that makes it
Form
tablet
Strength
200 mg
Approval
ANDA ANDA075389
On the market since
Apr 16, 2018
Package NDCs
51862-241-05 51862-241-60 51862-241-90
Official label
DailyMed (National Library of Medicine), updated Sep 4, 2025

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