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DONEPEZIL HYDROCHLORIDE
DONEPEZIL HYDROCHLORIDE - 24724-029-01 - (DONEPEZIL)
Drug Information of DONEPEZIL HYDROCHLORIDE
| Product NDC: | 24724-029 |
| Proprietary Name: | DONEPEZIL HYDROCHLORIDE |
| Non Proprietary Name: | DONEPEZIL |
| Active Ingredient(s): | 10 mg/1 & nbsp; DONEPEZIL |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DONEPEZIL HYDROCHLORIDE
| Product NDC: | 24724-029 |
| Labeler Name: | INDICUS PHARMA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201634 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110615 |
Package Information of DONEPEZIL HYDROCHLORIDE
| Package NDC: | 24724-029-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BLISTER PACK (24724-029-01) |
NDC Information of DONEPEZIL HYDROCHLORIDE
| NDC Code | 24724-029-01 |
| Proprietary Name | DONEPEZIL HYDROCHLORIDE |
| Package Description | 100 TABLET, FILM COATED in 1 BLISTER PACK (24724-029-01) |
| Product NDC | 24724-029 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DONEPEZIL |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110615 |
| Marketing Category Name | ANDA |
| Labeler Name | INDICUS PHARMA LLC |
| Substance Name | DONEPEZIL HYDROCHLORIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |
