NDC 59579-006

Air 1000 mL per 1 L gas

On the label: Linde Gas & Equipment Inc..

United States: 15

Where it's made

FactoryWhereRoleLast FDA inspection
Linde Gas & Equipment Inc.Tacoma, WA, United StatesMakes it No problems foundApr 8, 2014 · 3 inspections
Linde Gas & Equipment Inc.Cudahy, CA, United StatesMakes it Not inspected on record
Linde Gas & Equipment Inc.Canton, MI, United StatesMakes it No problems foundOct 9, 2014 · 1 inspection
Linde Gas & Equipment Inc.North Royalton, OH, United StatesMakes it No problems foundMar 11, 2014 · 1 inspection
Linde Gas & Equipment Inc.Slatersville, RI, United StatesMakes it Problems found, fixed voluntarilyApr 23, 2014 · 1 inspection
Linde Gas & Equipment Inc.Brookfield, WI, United StatesMakes it No problems foundJan 29, 2013 · 1 inspection
Linde Gas & Equipment Inc.Cahokia, IL, United StatesMakes it No problems foundMar 18, 2016 · 2 inspections
Linde Gas & Equipment Inc.Hillside, IL, United StatesMakes it Problems found, fixed voluntarilySep 19, 2024 · 2 inspections
Linde Gas & Equipment Inc.Roseville, MN, United StatesMakes it Problems found, fixed voluntarilySep 18, 2015 · 1 inspection
Linde Gas & Equipment Inc.Wilmington, OH, United StatesMakes it Not inspected on record
Linde Gas & Equipment Inc.Morrisville, PA, United StatesMakes it Problems found, fixed voluntarilyApr 1, 2026 · 2 inspections
Linde Gas & Equipment Inc.Pittsburg, CA, United StatesMakes it No problems foundNov 1, 2013 · 2 inspections
Linde Gas & Equipment Inc.Houston, TX, United StatesMakes it Not inspected on record
Linde Gas & Equipment Inc.Phoenix, AZ, United StatesMakes it Problems found, fixed voluntarilyJul 24, 2026 · 2 inspections
Linde Gas & Equipment Inc.Twinsburg, OH, United StatesMakes it No problems foundNov 20, 2019 · 2 inspections

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Air: every company that makes it
Form
gas, respiratory (inhalation)
Strength
1000 mL per 1 L
Approval
NDA NDA205910
On the market since
May 1, 2002
Package NDCs
59579-006-01 59579-006-02 59579-006-03 59579-006-04 59579-006-05 59579-006-06 59579-006-07 59579-006-08 59579-006-09 59579-006-10 59579-006-11 59579-006-12
Official label
DailyMed (National Library of Medicine), updated Jan 27, 2025

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