FDA NDC Directory · JSON-LD · Markdown

albuterol sulfate

NDC 53489-176 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA072637
Dosage form / routeTABLET · ORAL
Active ingredientsALBUTEROL SULFATE (2 mg/1)
Marketing started19891205
Package count5

External sources

Source: openFDA. Public-domain (CC0).