FDA.reportPublic FDA data

NDC 67871-772 - GLOFIL-125

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
67871-772
Package NDCs from labels
67871-772-92
Manufacturer
QOL Medical
Effective date
2007-06-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
GLOFIL-125 - QOL MedicalQOL Medical2007-06-23HUMAN PRESCRIPTION DRUG LABELING

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Iothalamate sodium, I-125ACTIVE INGREDIENT31J5U3Q9ZNGLOFIL-125 (IOTHALAMATE SODIUM, I-125) INJECTION [QOL MEDICAL]1
Iothalamate sodium, I-125ACTIVE MOIETY31J5U3Q9ZNGLOFIL-125 (IOTHALAMATE SODIUM, I-125) INJECTION [QOL MEDICAL]1
benzyl alcoholINACTIVE INGREDIENTLKG8494WBHGLOFIL-125 (IOTHALAMATE SODIUM, I-125) INJECTION [QOL MEDICAL]1
hydrochloric acidINACTIVE INGREDIENTQTT17582CBGLOFIL-125 (IOTHALAMATE SODIUM, I-125) INJECTION [QOL MEDICAL]1
sodium bicarbonateINACTIVE INGREDIENT8MDF5V39QOGLOFIL-125 (IOTHALAMATE SODIUM, I-125) INJECTION [QOL MEDICAL]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 1 of 1 ยท 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5680FB25-E286-2B0D-DBCD-A28D53D2B8F02C07CE91-CC83-45e3-BD2B-F923A9C8286C2007-06-23Warnings, Adverse reactionsExact identifier
spl id: 5680FB25-E286-2B0D-DBCD-A28D53D2B8F0
spl set id: 2C07CE91-CC83-45e3-BD2B-F923A9C8286C

Reported adverse events (FAERS/openFDA)#

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