High Outlier
Strength
300 mg/1
Manufacturer
ANI Pharmaceuticals, Inc.NDC
62559028001
Classification
Brand
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
LITHIUM CARBONATEApproval Type
New Drug (NDA)
FDA Application
NDA018027On Market Since
7/1/2014
Pharmacological Classes
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