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DONEPEZIL HYDROCHLORIDE - 24724-028-01 - (DONEPEZIL)

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Drug Information of DONEPEZIL HYDROCHLORIDE

Product NDC: 24724-028
Proprietary Name: DONEPEZIL HYDROCHLORIDE
Non Proprietary Name: DONEPEZIL
Active Ingredient(s): 5    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: 24724-028
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: 24724-028-01
Package Description: 100 TABLET, FILM COATED in 1 BLISTER PACK (24724-028-01)

NDC Information of DONEPEZIL HYDROCHLORIDE

NDC Code 24724-028-01
Proprietary Name DONEPEZIL HYDROCHLORIDE
Package Description 100 TABLET, FILM COATED in 1 BLISTER PACK (24724-028-01)
Product NDC 24724-028
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 5
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of DONEPEZIL HYDROCHLORIDE


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