FDA NDC Directory · JSON-LD · Markdown

Albuterol Sulfate

NDC 68788-8874 · HUMAN PRESCRIPTION DRUG · INHALANT

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209959
Dosage form / routeINHALANT · RESPIRATORY (INHALATION)
Active ingredientsALBUTEROL SULFATE (90 ug/1)
Marketing started20250516
Package count1

External sources

Source: openFDA. Public-domain (CC0).