FDA NDC Directory · JSON-LD · Markdown

ALBUTEROL SULFATE

NDC 70752-102 · HUMAN PRESCRIPTION DRUG · SYRUP

Labeler / ManufacturerQUAGEN PHARMACEUTICALS LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212197
Dosage form / routeSYRUP · ORAL
Active ingredientsALBUTEROL SULFATE (2 mg/5mL)
Marketing started20190906
Package count1

External sources

Source: openFDA. Public-domain (CC0).