NDC 0409-3435-01 - Fluconazole

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
0409-3435
Requested NDC
0409-3435-01
Package NDCs from labels
0409-3435-01, 0409-3435-24
Manufacturer
Hospira, Inc | InfoRLife SA | Infomed Fluids Srl
Effective date
2024-12-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Fluconazole - Hospira, Inc | InfoRLife SA | Infomed Fluids SrlHospira, Inc | InfoRLife SA | Infomed Fluids Srl2024-12-05HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0409-3435-01Fluconazole1 in 1 POUCHINJECTION, SOLUTION12
0409-3435-01Fluconazole100 mL in 1 BAGINJECTION, SOLUTION1002
0409-3435-24Fluconazole24 in 1 CARTONINJECTION, SOLUTION242

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0409-3435FLUCONAZOLE INJECTION, SOLUTION [HOSPIRA, INC]2Current NDC, 3 package rows20250107_22ebc3fb-ee81-44bd-a6e3-5e759ee724a8.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0409-3435-01ML - Milliliter0409-343536a44253-5845-49c0-b4ed-582b96c4f80212025-02-10
0409-3435-24ML - Milliliter0409-343597f0e8ed-cbfa-48d5-936a-0baa40c031bf12025-02-10

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 54 of 54 · 1,061 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: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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