NDC 49480-003 - ALFAXAN MULTIDOSE IDX

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
49480-003
Package NDCs from labels
49480-003-01, 49480-003-02
Manufacturer
Jurox Pty. Limited
Effective date
2024-02-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ALFAXAN MULTIDOSE IDX - Jurox Pty. LimitedJurox Pty. Limited2024-02-05PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49480-003-01ALFAXANMULTIDOSE IDX1 in 1 CARTONSOLUTION13
49480-003-01ALFAXANMULTIDOSE IDX10 mL in 1 VIAL, GLASSSOLUTION103
49480-003-02ALFAXANMULTIDOSE IDX1 in 1 CARTONSOLUTION13
49480-003-02ALFAXANMULTIDOSE IDX20 mL in 1 VIAL, GLASSSOLUTION203

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49480-003ALFAXAN MULTIDOSE IDX (ALFAXALONE) SOLUTION [JUROX PTY. LIMITED]34 package rows20240206_6fd00f51-db05-407f-ab80-cba1b6aa9596.zip

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 188 of 188 · 3,742 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RingersSODIUM CHLORIDE, CALCIUM CHLORIDE, POTASSIUM CHLORIDE,Baxter Healthcare Corporatione1953d54-818d-46a6-8532-518ebae6d84e2012-06-13Exact identifier
unii: 451W47IQ8X
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.