FDA NDC Directory · JSON-LD · Markdown

Albuterol Sulfate

NDC 62135-672 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA072151
Dosage form / routeTABLET · ORAL
Active ingredientsALBUTEROL SULFATE (4 mg/1)
Marketing started19891205
Package count1

External sources

Source: openFDA. Public-domain (CC0).