FDA NDC Directory · JSON-LD · Markdown

Terbutaline Sulfate

NDC 71205-939 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA211832
Dosage form / routeTABLET · ORAL
Active ingredientsTERBUTALINE SULFATE (5 mg/1)
Marketing started20200713
Package count5

External sources

Source: openFDA. Public-domain (CC0).