Product NDC: | 67046-489 |
Proprietary Name: | Namenda |
Non Proprietary Name: | memantine hydrochloride |
Active Ingredient(s): | 10 mg/1 & nbsp; memantine hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67046-489 |
Labeler Name: | Contract Pharmacy Services-PA |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021487 |
Marketing Category: | NDA |
Start Marketing Date: | 20100319 |
Package NDC: | 67046-489-60 |
Package Description: | 60 TABLET in 1 BLISTER PACK (67046-489-60) |
NDC Code | 67046-489-60 |
Proprietary Name | Namenda |
Package Description | 60 TABLET in 1 BLISTER PACK (67046-489-60) |
Product NDC | 67046-489 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | memantine hydrochloride |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100319 |
Marketing Category Name | NDA |
Labeler Name | Contract Pharmacy Services-PA |
Substance Name | MEMANTINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | NMDA Receptor Antagonists [MoA],N-methyl-D-aspartate Receptor Antagonist [EPC] |