NDC 71872-7054-01 - 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: 71872-7054
Requested NDC: 71872-7054-01
Package NDCs from labels: 71872-7054-1, 71872-7054-01
Manufacturer: Medical Purchasing Solutions, LLC
Effective date: 2023-05-30
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 - Medical Purchasing Solutions, LLC	Medical Purchasing Solutions, LLC	2023-05-30	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71872-7054-1	Albuterol Sulfate	1 in 1 BAG	SOLUTION	1		3
71872-7054-1	Albuterol Sulfate	3 mL in 1 AMPULE	SOLUTION	3		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71872-7054	ALBUTEROL SULFATE SOLUTION [MEDICAL PURCHASING SOLUTIONS, LLC]	3	Current NDC, Legacy NDC, 2 package rows	20230531_6a4b4b95-d1d3-9051-e053-2a91aa0a52e8.zip

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 7 of 7 · 121 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ipratropium Bromide and Albuterol Sulfate	IPRATROPIUM BROMIDE AND ALBUTEROL SULFATE	Mylan Pharmaceuticals Inc.	23c05e9a-9df5-4978-8831-cf562aa4ba92	2018-12-12	Warnings, Adverse reactions	Exact identifier unii: 021SEF3731

Reported adverse events (FAERS/openFDA)#

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