High Outlier
Strength
200 mg/1
Manufacturer
Dr. Reddy's Laboratories Inc.NDC
43598072101
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
HYDROXYCHLOROQUINE SULFATEApproval Type
Generic (ANDA)
FDA Application
ANDA210441On Market Since
5/1/2018
Pharmacological Classes
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