Strength
200 mg/1
Manufacturer
Aurobindo Pharma LimitedNDC
59651088905
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
HYDROXYCHLOROQUINE SULFATEApproval Type
Generic (ANDA)
FDA Application
ANDA040274On Market Since
3/7/2025
Pharmacological Classes
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