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ALBUTEROL SULFATE

NDC 51662-1513 · HUMAN PRESCRIPTION DRUG · AEROSOL, METERED

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA203760
Dosage form / routeAEROSOL, METERED · RESPIRATORY (INHALATION)
Active ingredientsALBUTEROL SULFATE (90 ug/1)
Marketing started20200818
Package count1

External sources

Source: openFDA. Public-domain (CC0).