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Albuterol

NDC 70710-1062 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208884
Dosage form / routeTABLET · ORAL
Active ingredientsALBUTEROL SULFATE (4 mg/1)
Marketing started20201023
Package count2

External sources

Source: openFDA. Public-domain (CC0).