FDA NDC Directory · JSON-LD · Markdown

Albuterol

NDC 71205-899 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namealbuterol
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA207046
Dosage form / routeTABLET · ORAL
Active ingredientsALBUTEROL SULFATE (4 mg/1)
Marketing started20180629
Package count6

External sources

Source: openFDA. Public-domain (CC0).