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Aricept
Aricept - 54868-3952-0 - (donepezil hydrochloride)
Drug Information of Aricept
| Product NDC: | 54868-3952 |
| Proprietary Name: | Aricept |
| Non Proprietary Name: | donepezil hydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; donepezil hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aricept
| Product NDC: | 54868-3952 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020690 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080509 |
Package Information of Aricept
| Package NDC: | 54868-3952-0 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (54868-3952-0) |
NDC Information of Aricept
| NDC Code | 54868-3952-0 |
| Proprietary Name | Aricept |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (54868-3952-0) |
| Product NDC | 54868-3952 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | donepezil hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20080509 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | DONEPEZIL HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |
