NDC 68382-522

Propafenone Hydrochloride 225 mg capsule, extended release

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 voluntarilyMar 24, 2023 · 5 inspections

Product details

Generic drug
Propafenone: every company that makes it
Form
capsule, extended release, oral
Strength
225 mg
Approval
ANDA ANDA214184
On the market since
Feb 2, 2022
Package NDCs
68382-522-05 68382-522-14
Official label
DailyMed (National Library of Medicine), updated Mar 23, 2024

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