NDC 62856-851-30 - ARICEPT

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
62856-851
Requested NDC
62856-851-30
Package NDCs from labels
62856-851-30
Manufacturer
Eisai Inc.
Effective date
2007-05-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ARICEPT® Oral Solution (Donepezil Hydrochloride)Eisai Inc.2007-05-24HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62856-851-30ARICEPT300 mL in 1 BOTTLE, PLASTICSOLUTION3001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62856-851ARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]11 package rows20070531_2B1B7B5F-2F20-418C-B1AC-794C2EF1CE5E.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
donepezil hydrochlorideACTIVE INGREDIENT3O2T2PJ89DARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1
donepezilACTIVE MOIETY8SSC91326PARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1
citric acid anhydrousINACTIVE INGREDIENT2968PHW8QPARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1
methylparabenINACTIVE INGREDIENTARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1
povidone K-30INACTIVE INGREDIENTARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1
propylene glycolINACTIVE INGREDIENT6DC9Q167V3ARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1
sodium benzoateINACTIVE INGREDIENTOJ245FE5EUARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1
sodium citrate dihydrateINACTIVE INGREDIENTB22547B95KARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1
sodium metabisulfiteINACTIVE INGREDIENTARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1
sorbitolINACTIVE INGREDIENT506T60A25RARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1
strawberry flavorINACTIVE INGREDIENTARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1
waterINACTIVE INGREDIENT059QF0KO0RARICEPT (DONEPEZIL HYDROCHLORIDE) SOLUTION [EISAI INC.]1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
E6D28BF2-7C39-256A-3930-39B48D367FBE2B1B7B5F-2F20-418C-B1AC-794C2EF1CE5E2007-05-24Warnings, Adverse reactionsExact identifier
spl id: E6D28BF2-7C39-256A-3930-39B48D367FBE
spl set id: 2B1B7B5F-2F20-418C-B1AC-794C2EF1CE5E

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.