FDA NDC Directory · JSON-LD · Markdown

Albuterol

NDC 69238-1344 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208804
Dosage form / routeTABLET · ORAL
Active ingredientsALBUTEROL SULFATE (2 mg/1)
Marketing started20180524
Package count2

External sources

Source: openFDA. Public-domain (CC0).