NDC 82009-045

Hydroxychloroquine sulfate 200 mg tablet, film coated

On the label: Quallent Pharmaceuticals Health LLC.

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
Hydroxychloroquine: every company that makes it
Form
tablet, film coated, oral
Strength
200 mg
Approval
ANDA ANDA040657
On the market since
Sep 30, 2022
Package NDCs
82009-045-05
Official label
DailyMed (National Library of Medicine), updated Dec 21, 2023

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