FDA.reportPublic FDA data

NDC 11098-030 - SUBLIMAZE

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
11098-030
Package NDCs from labels
11098-030-02, 11098-030-05, 11098-030-10, 11098-030-20
Manufacturer
Taylor Pharmaceuticals
Effective date
2008-04-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SUBLIMAZE - Taylor PharmaceuticalsTaylor Pharmaceuticals2008-04-21HUMAN PRESCRIPTION DRUG LABELING

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
fentanyl citrateACTIVE INGREDIENTMUN5LYG46HSUBLIMAZE (FENTANYL CITRATE) INJECTION, SOLUTION [TAYLOR PHARMACEUTICALS]1
fentanylACTIVE MOIETYUF599785JZSUBLIMAZE (FENTANYL CITRATE) INJECTION, SOLUTION [TAYLOR PHARMACEUTICALS]1
sodium hydroxideINACTIVE INGREDIENT55X04QC32ISUBLIMAZE (FENTANYL CITRATE) INJECTION, SOLUTION [TAYLOR PHARMACEUTICALS]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
E7FCE1EB-443E-B5AA-4E29-5E8376E4D05A8944EA18-016E-4971-876D-2365FAC190EA2008-04-21Warnings, Adverse reactionsExact identifier
spl id: E7FCE1EB-443E-B5AA-4E29-5E8376E4D05A
spl set id: 8944EA18-016E-4971-876D-2365FAC190EA

Reported adverse events (FAERS/openFDA)#

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