Namenda - 63629-3383-2 - (memantine hydrochloride)

Alphabetical Index


Drug Information of Namenda

Product NDC: 63629-3383
Proprietary Name: Namenda
Non Proprietary Name: memantine hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   memantine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Namenda

Product NDC: 63629-3383
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021487
Marketing Category: NDA
Start Marketing Date: 20031016

Package Information of Namenda

Package NDC: 63629-3383-2
Package Description: 60 TABLET in 1 BOTTLE (63629-3383-2)

NDC Information of Namenda

NDC Code 63629-3383-2
Proprietary Name Namenda
Package Description 60 TABLET in 1 BOTTLE (63629-3383-2)
Product NDC 63629-3383
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name memantine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20031016
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name MEMANTINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes NMDA Receptor Antagonists [MoA],N-methyl-D-aspartate Receptor Antagonist [EPC]

Complete Information of Namenda


General Information