NDC 59930-1560-1 - 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: 59930-1560-1
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
Label	Manufacturer	Effective date	Type
Albuterol - Warrick Pharmaceuticals Corporation	Warrick Pharmaceuticals Corporation	2006-12-07	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59930-1560-1	Albuterol	200 in 1 INHALER	AEROSOL, SPRAY	200		1
59930-1560-2	Albuterol	200 in 1 INHALER, REFILL	AEROSOL, SPRAY	200		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59930-1560	ALBUTEROL (ALBUTEROL) AEROSOL, SPRAY [WARRICK PHARMACEUTICALS CORPORATION]	1	2 package rows	20070126_A000ABB9-92A1-4C84-8932-CD40C476DC00.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Albuterol	ACTIVE INGREDIENT	QF8SVZ843E	ALBUTEROL (ALBUTEROL) AEROSOL, SPRAY [WARRICK PHARMACEUTICALS CORPORATION]	1
Albuterol	ACTIVE MOIETY	QF8SVZ843E	ALBUTEROL (ALBUTEROL) AEROSOL, SPRAY [WARRICK PHARMACEUTICALS CORPORATION]	1
dichlorodifluoromethasone	INACTIVE INGREDIENT		ALBUTEROL (ALBUTEROL) AEROSOL, SPRAY [WARRICK PHARMACEUTICALS CORPORATION]	1
oleic acid	INACTIVE INGREDIENT	2UMI9U37CP	ALBUTEROL (ALBUTEROL) AEROSOL, SPRAY [WARRICK PHARMACEUTICALS CORPORATION]	1
trichloromonofluoromethane	INACTIVE INGREDIENT		ALBUTEROL (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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
A000ABB9-92A1-4C84-8932-CD40C476DC00			A000ABB9-92A1-4C84-8932-CD40C476DC00	2006-12-07	Warnings, Adverse reactions	Exact 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.