FDA NDC Directory · JSON-LD · Markdown

Albuterol

NDC 64980-442 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namealbuterol
Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207046
Dosage form / routeTABLET · ORAL
Active ingredientsALBUTEROL SULFATE (2 mg/1)
Marketing started20180629
Package count2

External sources

Source: openFDA. Public-domain (CC0).