NDC 58468-0229 - Cablivi

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
58468-0229
Package NDCs from labels
58468-0229-1
Manufacturer
Genzyme Corporation | Richter Helm Biologics GmbH and Co KG (Bovenau) | Richter Helm Biologics GmbH and Co KG (Hamburg) | Patheon Italia S.p.A. | Ablynx | Enestia Belgium NV (trading as Sharp Packaging Solutions)
Effective date
2026-04-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
CabliviGenzyme Corporation | Richter Helm Biologics GmbH and Co KG (Bovenau) | Richter Helm Biologics GmbH and Co KG (Hamburg) | Patheon Italia S.p.A. | Ablynx | Enestia Belgium NV (trading as Sharp Packaging Solutions)2026-04-24HUMAN PRESCRIPTION DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58468-0229CABLIVI (CAPLACIZUMAB) KIT [GENZYME CORPORATION]14Unmatched20241108_2348f06e-8004-4040-832e-e9e86a39f905.zip

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 18 of 18 · 343 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Eye WashWATERCVS Pharmacy049cee29-7ec2-4d5b-8308-f522acde43a72017-03-29WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
CPDA-1ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINEFenwal, Inc.051f7347-5a76-4664-8fe2-e61b3dfcb0e42014-08-27Exact identifier
unii: XF417D3PSL
unii: B22547B95K

Reported adverse events (FAERS/openFDA)#

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