FDA.reportPublic FDA data

NDC 66658-112-01

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
66658-112
Requested NDC
66658-112-01
Package NDCs from labels
66658-112-01
Manufacturer
National Council for Prescription Drug Programs
Effective date
2013-02-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
National Council for Prescription Drug Programs indexing - billing unitNational Council for Prescription Drug Programs2013-02-13Indexing - Billing Unit

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66658-112-01EA - Each66658-1128e662888-3652-4e21-bf83-e2d1b055340c12013-02-13
66658-112-03EA - Each66658-112833670be-d969-416e-9939-047f98c26b4c12012-07-24
66658-112-06EA - Each66658-112e86d693e-4c82-4407-8f08-e5434c6a8a9412012-07-24

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 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
KEPIVANCEPALIFERMINSwedish Orphan Biovitrum AB (publ)426f6e64-2c20-4a61-6d65-7320426f6e642025-12-17Warnings, Adverse reactionsExact identifier
application number: BLA125103

Reported adverse events (FAERS/openFDA)#

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