NDC 0615-8459

Hydroxychloroquine sulfate 200 mg tablet, film coated

On the label: NCS HealthCare of KY, Inc dba Vangard Labs. It's repackaged: NCS HealthCare of KY, Inc dba Vangard Labs rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-096.

India: 2

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Zydus Lifesciences LimitedAhmedabad, IndiaMakes it and tests it Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action
Zydus Lifesciences LimitedSolan, IndiaMakes it and tests it No problems foundMar 9, 2020 · 6 inspections

Repackaging site

Product details

Generic drug
Hydroxychloroquine: every company that makes it
Form
tablet, film coated, oral
Strength
200 mg
Approval
ANDA ANDA040657
On the market since
Jan 3, 2008
Package NDCs
0615-8459-39
Official label
DailyMed (National Library of Medicine), updated Jun 21, 2024

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