FDA.reportPublic FDA data

NDC 59930-1560-2 - Albuterol

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
59930-1560
Requested NDC
59930-1560-2
Package NDCs from labels
59930-1560-1, 59930-1560-2
Manufacturer
Warrick Pharmaceuticals Corporation
Effective date
2006-12-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Albuterol - Warrick Pharmaceuticals CorporationWarrick Pharmaceuticals Corporation2006-12-07HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59930-1560-1Albuterol200 in 1 INHALERAEROSOL, SPRAY2001
59930-1560-2Albuterol200 in 1 INHALER, REFILLAEROSOL, SPRAY2001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59930-1560ALBUTEROL (ALBUTEROL) AEROSOL, SPRAY [WARRICK PHARMACEUTICALS CORPORATION]12 package rows20070126_A000ABB9-92A1-4C84-8932-CD40C476DC00.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AlbuterolACTIVE INGREDIENTQF8SVZ843EALBUTEROL (ALBUTEROL) AEROSOL, SPRAY [WARRICK PHARMACEUTICALS CORPORATION]1
AlbuterolACTIVE MOIETYQF8SVZ843EALBUTEROL (ALBUTEROL) AEROSOL, SPRAY [WARRICK PHARMACEUTICALS CORPORATION]1
dichlorodifluoromethasoneINACTIVE INGREDIENTALBUTEROL (ALBUTEROL) AEROSOL, SPRAY [WARRICK PHARMACEUTICALS CORPORATION]1
oleic acidINACTIVE INGREDIENT2UMI9U37CPALBUTEROL (ALBUTEROL) AEROSOL, SPRAY [WARRICK PHARMACEUTICALS CORPORATION]1
trichloromonofluoromethaneINACTIVE INGREDIENTALBUTEROL (ALBUTEROL) AEROSOL, SPRAY [WARRICK PHARMACEUTICALS CORPORATION]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
A000ABB9-92A1-4C84-8932-CD40C476DC00A000ABB9-92A1-4C84-8932-CD40C476DC002006-12-07Warnings, Adverse reactionsExact identifier
spl id: A000ABB9-92A1-4C84-8932-CD40C476DC00
spl set id: A000ABB9-92A1-4C84-8932-CD40C476DC00

Reported adverse events (FAERS/openFDA)#

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