Product NDC: | 0456-3200 |
Proprietary Name: | Namenda |
Non Proprietary Name: | Memantine Hydrochloride |
Active Ingredient(s): | & nbsp; Memantine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0456-3200 |
Labeler Name: | Forest Laboratories, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021487 |
Marketing Category: | NDA |
Start Marketing Date: | 20031016 |
Package NDC: | 0456-3200-14 |
Package Description: | 1 KIT in 1 BLISTER PACK (0456-3200-14) |
NDC Code | 0456-3200-14 |
Proprietary Name | Namenda |
Package Description | 1 KIT in 1 BLISTER PACK (0456-3200-14) |
Product NDC | 0456-3200 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Memantine Hydrochloride |
Dosage Form Name | KIT |
Route Name | ORAL |
Start Marketing Date | 20031016 |
Marketing Category Name | NDA |
Labeler Name | Forest Laboratories, Inc. |
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