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 | Type |
|---|---|---|---|
| ARICEPT® Oral Solution (Donepezil Hydrochloride) | Eisai Inc. | 2007-05-24 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62856-851-30 | ARICEPT | 300 mL in 1 BOTTLE, PLASTIC | SOLUTION | 300 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| E6D28BF2-7C39-256A-3930-39B48D367FBE | 2B1B7B5F-2F20-418C-B1AC-794C2EF1CE5E | 2007-05-24 | Warnings, Adverse reactions | E6D28BF2-7C39-256A-3930-39B48D367FBE 2B1B7B5F-2F20-418C-B1AC-794C2EF1CE5E |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.