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donepezil hydrochloride
donepezil hydrochloride - 63739-652-10 - (donepezil hydrochloride)
Drug Information of donepezil hydrochloride
| Product NDC: | 63739-652 |
| Proprietary Name: | donepezil hydrochloride |
| Non Proprietary Name: | donepezil hydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; donepezil hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of donepezil hydrochloride
| Product NDC: | 63739-652 |
| Labeler Name: | McKesson Packaging Services a business unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090175 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130308 |
Package Information of donepezil hydrochloride
| Package NDC: | 63739-652-10 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-652-10) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
NDC Information of donepezil hydrochloride
| NDC Code | 63739-652-10 |
| Proprietary Name | donepezil hydrochloride |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-652-10) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| Product NDC | 63739-652 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | donepezil hydrochloride |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20130308 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Packaging Services a business unit of McKesson Corporation |
| Substance Name | DONEPEZIL HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |
