Active Ingredient: MEMANTINE HYDROCHLORIDE
Proprietary Name: MEMANTINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A090041
Product Number: 002
Approval Date: Apr 10, 2015
Applicant Holder Full Name: AMNEAL PHARMACEUTICALS OF NEW YORK LLC
Marketing Status:
Prescription
Patent and Exclusivity Information