NDC 67457-209 - Dexrazoxane Hydrochloride

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
67457-209
Package NDCs from labels
67457-209-50
Manufacturer
Mylan Institutional LLC
Effective date
2018-04-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Dexrazoxane Hydrochloride - Mylan Institutional LLCMylan Institutional LLC2018-04-16HUMAN PRESCRIPTION DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DEXRAZOXANE HYDROCHLORIDEACTIVE INGREDIENT5346058Q7SDEXRAZOXANE HYDROCHLORIDE (DEXRAZOXANE) KIT [MYLAN INSTITUTIONAL LLC]5
DEXRAZOXANEACTIVE MOIETY048L81261FDEXRAZOXANE HYDROCHLORIDE (DEXRAZOXANE) KIT [MYLAN INSTITUTIONAL LLC]5
HYDROCHLORIC ACIDINACTIVE INGREDIENTQTT17582CBDEXRAZOXANE HYDROCHLORIDE (DEXRAZOXANE) KIT [MYLAN INSTITUTIONAL LLC]5

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 5 of 5 · 81 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lactated RingersSODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDEBaxter Healthcare Corporationf09f80bf-2f8b-4420-865d-aec2d5e5cd4d2012-06-12Exact identifier
unii: TU7HW0W0QT

Reported adverse events (FAERS/openFDA)#

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