Strength
20 mg/1
Manufacturer
Camber Pharmaceuticals Inc.NDC
31722008030
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
LURASIDONE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA218174On Market Since
8/21/2024
Pharmacological Classes
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