FDA.reportPublic FDA data

NDC 76179-025-01 - KEDBUMIN

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
76179-025
Requested NDC
76179-025-01
Package NDCs from labels
76179-025-01, 76179-025-02, 76179-025-03, 76179-025-04
Manufacturer
Kedrion S.p.A
Effective date
2026-08-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
KEDBUMIN - Kedrion S.p.AKedrion S.p.A2026-08-20PLASMA DERIVATIVE
National Council for Prescription Drug Programs indexing - billing unitNational Council for Prescription Drug Programs2012-07-24Indexing - Billing Unit

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76179-025-01KEDBUMIN50 mL in 1 VIAL, GLASSINJECTION, SOLUTION5017
76179-025-02KEDBUMIN1 in 1 CARTONINJECTION, SOLUTION117
76179-025-03KEDBUMIN100 mL in 1 VIALINJECTION, SOLUTION10017
76179-025-04KEDBUMIN1 in 1 CARTONINJECTION, SOLUTION117

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76179-025KEDBUMIN (ALBUMIN (HUMAN)) INJECTION, SOLUTION [KEDRION S.P.A]16Current NDC, Legacy NDC, 4 package rows20230928_57bd6811-8619-11e0-9d78-0800200c9a66.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
76179-025-01ML - Milliliter76179-02505a1c14e-bbbb-428e-bb94-395b1934e49012012-07-24
76179-025-02ML - Milliliter76179-0250cca745e-4bcc-4f7b-b6c3-914819a3db0712013-02-13
76179-025-03ML - Milliliter76179-0250bd3d118-25b3-4614-8763-5500963863de12013-08-02
76179-025-04ML - Milliliter76179-025ea54b735-fc02-4044-98e8-498400f8981b12013-08-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALBUMIN (HUMAN)ACTIVE INGREDIENTZIF514RVZRKEDBUMIN (ALBUMIN (HUMAN)) INJECTION, SOLUTION [KEDRION S.P.A]9
ALBUMIN (HUMAN)ACTIVE MOIETYZIF514RVZRKEDBUMIN (ALBUMIN (HUMAN)) INJECTION, SOLUTION [KEDRION S.P.A]9

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 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Proteinuria Drops 2053PROTEINURIA DROPSProfessional Complementary Health Formulas1bf80282-8283-4835-acd4-fbdb47788c672026-01-08WarningsExact identifier
unii: ZIF514RVZR
ALBUMINEXALBUMIN HUMANBPL8428d373-f4b1-4e3b-bb19-ea89048f7c792024-12-31Warnings, Adverse reactionsExact identifier
unii: ZIF514RVZR
ALBUMINEXALBUMIN HUMANBPL167f48d0-8ae5-4f7e-b050-9673dad78acc2024-12-31Warnings, Adverse reactionsExact identifier
unii: ZIF514RVZR

Reported adverse events (FAERS/openFDA)#

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