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donepezil hydrochloride
donepezil hydrochloride - 59762-0246-1 - (DONEPEZIL HYDROCHLORIDE)
Drug Information of donepezil hydrochloride
| Product NDC: | 59762-0246 |
| Proprietary Name: | donepezil hydrochloride |
| Non Proprietary Name: | DONEPEZIL HYDROCHLORIDE |
| Active Ingredient(s): | 10 mg/1 & nbsp; DONEPEZIL HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of donepezil hydrochloride
| Product NDC: | 59762-0246 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020690 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19961126 |
Package Information of donepezil hydrochloride
| Package NDC: | 59762-0246-1 |
| Package Description: | 1000 TABLET, FILM COATED in 1 BOTTLE (59762-0246-1) |
NDC Information of donepezil hydrochloride
| NDC Code | 59762-0246-1 |
| Proprietary Name | donepezil hydrochloride |
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (59762-0246-1) |
| Product NDC | 59762-0246 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DONEPEZIL HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19961126 |
| Marketing Category Name | NDA |
| Labeler Name | Greenstone LLC |
| Substance Name | DONEPEZIL HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |
