FDA NDC Directory · JSON-LD · Markdown

Albuterol Sulfate

NDC 0487-0301 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerNephron Pharmaceuticals Corporation
Marketing categoryAbbreviated NDA (generic) · App ANDA076355
Dosage form / routeSOLUTION · RESPIRATORY (INHALATION)
Active ingredientsALBUTEROL SULFATE (.63 mg/3mL)
Marketing started20100331
Package count1

External sources

Source: openFDA. Public-domain (CC0).