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LEVALBUTEROL

NDC 65862-942 · HUMAN PRESCRIPTION DRUG · SOLUTION, CONCENTRATE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA207628
Dosage form / routeSOLUTION, CONCENTRATE · RESPIRATORY (INHALATION)
Active ingredientsLEVALBUTEROL HYDROCHLORIDE (1.25 mg/.5mL)
Marketing started20170131
Package count1

External sources

Source: openFDA. Public-domain (CC0).