Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 090961

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MEMANTINE HYDROCHLORIDE (MEMANTINE HYDROCHLORIDE)
5MG
Marketing Status: Prescription

Active Ingredient: MEMANTINE HYDROCHLORIDE
Proprietary Name: MEMANTINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A090961
Product Number: 001
Approval Date: Jul 10, 2017
Applicant Holder Full Name: ZYDUS LIFESCIENCES LTD
Marketing Status:  Prescription
Patent and Exclusivity Information

MEMANTINE HYDROCHLORIDE (MEMANTINE HYDROCHLORIDE)
10MG
Marketing Status: Prescription

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: A090961
Product Number: 002
Approval Date: Jul 10, 2017
Applicant Holder Full Name: ZYDUS LIFESCIENCES LTD
Marketing Status:  Prescription
Patent and Exclusivity Information