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Namenda
Namenda - 0456-3200-14 - (Memantine Hydrochloride)
Drug Information of Namenda
| 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) |
Labeler Information of Namenda
| 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 Information of Namenda
| Package NDC: | 0456-3200-14 |
| Package Description: | 1 KIT in 1 BLISTER PACK (0456-3200-14) |
NDC Information of Namenda
| 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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