Active Ingredient: AMANTADINE HYDROCHLORIDE
Proprietary Name: AMANTADINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A212407
Product Number: 001
Approval Date: May 27, 2022
Applicant Holder Full Name: EDENBRIDGE PHARMACEUTICALS LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information