NDC 53489-176

albuterol sulfate 2 mg tablet

On the label: Caraco Pharmaceutical Laboratories, Ltd..

Hungary: 1United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
ALKALOIDA Vegyeszeti Gyar zartkoruen mukodo ReszvenytarsasagTiszavasvari, HungaryMakes it Problems found, fixed voluntarilyMar 12, 2025 · 6 inspections
Frontida BioPharm, LLCPhiladelphia, PA, United StatesMakes it No problems foundApr 2, 2026 · 10 inspections, 1 with FDA action

Product details

Generic drug
Albuterol: every company that makes it
Form
tablet, oral
Strength
2 mg
Approval
ANDA ANDA072637
On the market since
Dec 5, 1989
Package NDCs
53489-176-01 53489-176-02 53489-176-03 53489-176-05 53489-176-10
Official label
DailyMed (National Library of Medicine), updated Mar 16, 2026

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