NDC 17270-721 - 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: 17270-721
Package NDCs from labels: 17270-721-02
Manufacturer: Rebel Distributors Corp
Effective date: 2011-07-20
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Albuterol - Rebel Distributors Corp	Rebel Distributors Corp	2011-07-20	HUMAN PRESCRIPTION DRUG LABEL
Albuterol Inhalation Aerosol	Armstrong Pharmaceuticals, Inc.	2007-11-27	HUMAN PRESCRIPTION DRUG LABELING

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Albuterol	ACTIVE INGREDIENT	QF8SVZ843E	ALBUTEROL AEROSOL, METERED [REBEL DISTRIBUTORS CORP]	1
Albuterol	ACTIVE INGREDIENT	QF8SVZ843E	ALBUTEROL (ALBUTEROL) AEROSOL, METERED [ARMSTRONG PHARMACEUTICALS, INC.]	1
Albuterol	ACTIVE MOIETY	QF8SVZ843E	ALBUTEROL AEROSOL, METERED [REBEL DISTRIBUTORS CORP]	1
Albuterol	ACTIVE MOIETY	QF8SVZ843E	ALBUTEROL (ALBUTEROL) AEROSOL, METERED [ARMSTRONG PHARMACEUTICALS, INC.]	1
dichlorofluoromethane	INACTIVE INGREDIENT	7GAO4CRJ0B	ALBUTEROL AEROSOL, METERED [REBEL DISTRIBUTORS CORP]	1
dichlorofluoromethane	INACTIVE INGREDIENT	7GAO4CRJ0B	ALBUTEROL (ALBUTEROL) AEROSOL, METERED [ARMSTRONG PHARMACEUTICALS, INC.]	1
oleic acid	INACTIVE INGREDIENT	2UMI9U37CP	ALBUTEROL AEROSOL, METERED [REBEL DISTRIBUTORS CORP]	1
oleic acid	INACTIVE INGREDIENT	2UMI9U37CP	ALBUTEROL (ALBUTEROL) AEROSOL, METERED [ARMSTRONG PHARMACEUTICALS, INC.]	1
trichloromonoflueormethane	INACTIVE INGREDIENT		ALBUTEROL (ALBUTEROL) AEROSOL, METERED [ARMSTRONG PHARMACEUTICALS, INC.]	1
TRICHLOROMONOFLUOROMETHANE	INACTIVE INGREDIENT	990TYB331R	ALBUTEROL AEROSOL, METERED [REBEL DISTRIBUTORS CORP]	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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
3d02b370-0d4f-4aaa-b420-dc7366d19819			808e2b04-9e84-440a-b00e-2cbe858041da	2024-06-06	Boxed warning, Warnings, Adverse reactions	Exact identifier spl set id: 808e2b04-9e84-440a-b00e-2cbe858041da
29d24a6d-f9c1-4300-97c7-fec26bdbc22b			29d24a6d-f9c1-4300-97c7-fec26bdbc22b	2011-07-20	Boxed warning, Warnings, Adverse reactions	Exact identifier spl id: 29d24a6d-f9c1-4300-97c7-fec26bdbc22b spl set id: 29d24a6d-f9c1-4300-97c7-fec26bdbc22b

Reported adverse events (FAERS/openFDA)#

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