Strength
200 mg/1
Manufacturer
Zydus Pharmaceuticals (USA) Inc.NDC
68382009605
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
HYDROXYCHLOROQUINE SULFATEApproval Type
Generic (ANDA)
FDA Application
ANDA040657On Market Since
1/3/2008
Pharmacological Classes
HYDROXYCHLOROQUINE 200 MG TAB
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