Strength
200 mg/1
Manufacturer
Rising Pharma Holdings Inc.NDC
16571011201
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
HYDROXYCHLOROQUINE SULFATEApproval Type
Generic (ANDA)
FDA Application
ANDA210959On Market Since
5/29/2023
Pharmacological Classes
HYDROXYCHLOROQUINE 200 MG TAB
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