NDC 59930-1647-2 - Albuterol Sulfate

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: 59930-1647
Requested NDC: 59930-1647-2
Package NDCs from labels: 59930-1647-2
Manufacturer: Bausch & Lomb Incorporated
Effective date: 2008-09-02
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Albuterol Sulfate - Bausch & Lomb Incorporated	Bausch & Lomb Incorporated	2008-09-02	Human prescription drug label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59930-1647-2	Albuterol Sulfate	20 mL in 1 BOTTLE, GLASS	SOLUTION	20		1
59930-1647-2	Albuterol Sulfate	1 in 1 CARTON	SOLUTION	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59930-1647	ALBUTEROL SULFATE SOLUTION [BAUSCH & LOMB INCORPORATED]	1	2 package rows	20090105_D476C926-4C3D-4C33-B244-3B58E988ECB3.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ALBUTEROL SULFATE	ACTIVE INGREDIENT	021SEF3731	ALBUTEROL SULFATE SOLUTION [BAUSCH & LOMB INCORPORATED]	1
ALBUTEROL	ACTIVE MOIETY	QF8SVZ843E	ALBUTEROL SULFATE SOLUTION [BAUSCH & LOMB INCORPORATED]	1
Benzalkonium Chloride	INACTIVE INGREDIENT		ALBUTEROL SULFATE SOLUTION [BAUSCH & LOMB INCORPORATED]	1
Sulfuric Acid	INACTIVE INGREDIENT	O40UQP6WCF	ALBUTEROL SULFATE SOLUTION [BAUSCH & LOMB INCORPORATED]	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 · 5 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Albuterol Sulfate	ALBUTEROL SULFATE	Rising Pharma Holdings, Inc.	3236f82c-14e9-dfd4-e063-6294a90ac43d	2026-07-16	Warnings, Adverse reactions	Exact identifier rxcui: 245314
Albuterol Sulfate Inhalation Solution, 0.5%	ALBUTEROL SULFATE	Ritedose Pharmaceuticals, LLC	fdb4ac5a-bf0d-4896-89f7-1828c081b79e	2026-04-30	Warnings, Adverse reactions	Exact identifier rxcui: 245314
Albuterol Sulfate	ALBUTEROL SULFATE	Nephron Pharmaceuticals Corporation	ecc00500-58b8-491f-80df-dc6c89a08cae	2025-03-21	Warnings, Adverse reactions	Exact identifier rxcui: 245314
Albuterol Sulfate	ALBUTEROL SULFATE	Chartwell RX, LLC.	7f261a9b-65d9-408a-8609-c1b3809b8b4b	2024-02-21	Warnings, Adverse reactions	Exact identifier rxcui: 245314
2334D859-A344-13DD-4E29-C5F5DC5310BC			D476C926-4C3D-4C33-B244-3B58E988ECB3	2008-09-02	Warnings, Adverse reactions	Exact identifier spl id: 2334D859-A344-13DD-4E29-C5F5DC5310BC spl set id: D476C926-4C3D-4C33-B244-3B58E988ECB3

Reported adverse events (FAERS/openFDA)#

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