NDC 11098-010-01 - INAPSINE

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
11098-010
Requested NDC
11098-010-01
Package NDCs from labels
11098-010-01, 11098-010-02
Manufacturer
Taylor Pharmaceuticals
Effective date
2007-08-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
INAPSINE - Taylor PharmaceuticalsTaylor Pharmaceuticals2007-08-09HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11098-010-01INAPSINE1 mL in 1 AMPULEINJECTION11
11098-010-01INAPSINE10 in 1 PACKAGEINJECTION101
11098-010-02INAPSINE10 in 1 PACKAGEINJECTION101
11098-010-02INAPSINE2 mL in 1 AMPULEINJECTION21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11098-010INAPSINE (DROPERIDOL) INJECTION [TAYLOR PHARMACEUTICALS]14 package rows20080319_F4FA5E60-5F70-46D7-8E29-DFCF8B783F2C.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
droperidolACTIVE INGREDIENTO9U0F09D5XINAPSINE (DROPERIDOL) INJECTION [TAYLOR PHARMACEUTICALS]1
droperidolACTIVE MOIETYO9U0F09D5XINAPSINE (DROPERIDOL) INJECTION [TAYLOR PHARMACEUTICALS]1
lactic acidINACTIVE INGREDIENT33X04XA5ATINAPSINE (DROPERIDOL) INJECTION [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
E516A136-46DD-AF5A-4CC5-BC93BF8CF980F4FA5E60-5F70-46D7-8E29-DFCF8B783F2C2007-08-09Boxed warning, Warnings, Adverse reactionsExact identifier
spl id: E516A136-46DD-AF5A-4CC5-BC93BF8CF980
spl set id: F4FA5E60-5F70-46D7-8E29-DFCF8B783F2C

Reported adverse events (FAERS/openFDA)#

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