Strength
200 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
57664076188
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
2/21/2024
Active Ingredients
HYDROXYCHLOROQUINE SULFATEApproval Type
Generic (ANDA)
FDA Application
ANDA201691On Market Since
6/18/2018
Pharmacological Classes
HYDROXYCHLOROQUINE 200 MG TAB
Generic
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