FDA.reportPublic FDA data

CEFTIOFUR FREE ACID

Manufacturer
AMERICAN PHARMACEUTICAL INGREDIENTS LLC
Effective date
2014-03-25
Label type
BULK INGREDIENT
Version
2
Source
full-release
Hydrated at
2026-06-01 02:47:53

Label at a glance#

ProductCEFTIOFUR FREE ACID
Active ingredientCEFTIOFUR
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58597-8171-8CEFTIOFUR FREE ACID1000 g in 1 BOTTLEPOWDER10002
58597-8171-9CEFTIOFUR FREE ACID5000 g in 1 BOTTLEPOWDER50002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58597-8171CEFTIOFUR FREE ACID POWDER [AMERICAN PHARMACEUTICAL INGREDIENTS LLC]22 package rows20140325_1f3901d3-1138-4e97-933b-5c010284a0e1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CEFTIOFURACTIVE INGREDIENT83JL932I1C2
CEFTIOFURACTIVE MOIETY83JL932I1C2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58597-817158597-8171-8, 58597-8171-9

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
CEFTIOFUR83JL932I1CACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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