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Albuterol

NDC 69238-1345 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208804
Dosage form / routeTABLET · ORAL
Active ingredientsALBUTEROL SULFATE (4 mg/1)
Marketing started20180524
Package count2

External sources

Source: openFDA. Public-domain (CC0).