Strength
10 mg/1
Manufacturer
Viona Pharmaceuticals Inc.NDC
72578000405
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
MEMANTINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA090961On Market Since
2/28/2019
Pharmacological Classes
N-methyl-D-aspartate Receptor Antagonist
NMDA Receptor Antagonists
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