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Albuterol sulfate

NDC 70518-3541 · HUMAN PRESCRIPTION DRUG · AEROSOL, METERED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA209954
Dosage form / routeAEROSOL, METERED · RESPIRATORY (INHALATION)
Active ingredientsALBUTEROL SULFATE (90 ug/1)
Marketing started20220928
Package count1

External sources

Source: openFDA. Public-domain (CC0).