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Terbutaline Sulfate

NDC 71205-938 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA211832
Dosage form / routeTABLET · ORAL
Active ingredientsTERBUTALINE SULFATE (2.5 mg/1)
Marketing started20200713
Package count5

External sources

Source: openFDA. Public-domain (CC0).