Strength
200 mg/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
47335090518
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
2/18/2026
Active Ingredients
QUETIAPINE FUMARATEApproval Type
Generic (ANDA)
FDA Application
ANDA201190On Market Since
3/28/2012
Pharmacological Classes
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