FDA.reportPublic FDA data

NDC 76125-792-26 - ALBUKED

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
76125-792
Requested NDC
76125-792-26
Package NDCs from labels
76125-792-21, 76125-792-20, 76125-792-26, 76125-792-25, 76125-792-11, 76125-792-10
Manufacturer
A-S Medication Solutions
Effective date
2024-06-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ALBUKED - A-S Medication SolutionsA-S Medication Solutions2024-06-28PLASMA DERIVATIVE
Albuked - KEDRION BIOPHARMA, INC. | GRIFOLS THERAPEUTICS LLCKEDRION BIOPHARMA, INC. | GRIFOLS THERAPEUTICS LLC2020-08-01PLASMA DERIVATIVE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76125-792-10Albuked1 in 1 CARTONSOLUTION17
76125-792-11Albuked100 mL in 1 VIALSOLUTION1007
76125-792-20Albuked1 in 1 CARTONSOLUTION17
76125-792-21Albuked20 mL in 1 VIALSOLUTION207
76125-792-25Albuked1 in 1 CARTONSOLUTION17
76125-792-26Albuked50 mL in 1 VIALSOLUTION507

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76125-792ALBUKED (ALBUMIN (HUMAN)) SOLUTION [KEDRION BIOPHARMA, INC.]7Current NDC, Legacy NDC, 6 package rows20200804_face90dc-a227-3ec2-1645-f74eb9dac68c.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
76125-792-10ML - Milliliter76125-792bbd470f1-dae8-4861-987c-6d1d1a3e7ec412018-08-13
76125-792-11ML - Milliliter76125-792b3128bf4-809f-4eac-87dc-e148f9c4ede612018-08-13
76125-792-25ML - Milliliter76125-792facb884a-ab55-48ca-9be2-79f5b65d85ab12018-08-13
76125-792-26ML - Milliliter76125-7923dfa5a2a-419f-4d32-8435-f23d5a79e6ac12018-08-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Albumin (human)ACTIVE INGREDIENTZIF514RVZRALBUKED (ALBUMIN (HUMAN)) SOLUTION [KEDRION BIOPHARMA, INC]1
Albumin (human)ACTIVE MOIETYZIF514RVZRALBUKED (ALBUMIN (HUMAN)) SOLUTION [KEDRION BIOPHARMA, 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 9 of 9 · 164 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bio Rock WaterROCK WATERBioActive Nutritional, Inc.178bd16d-0d4f-49d8-866b-8ab3a3c6889d2018-07-30WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Corporationef3e79c5-3f58-4b36-a296-64b7d9a651c12017-10-17Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
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

Reported adverse events (FAERS/openFDA)#

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