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Terbutaline Sulfate

NDC 0404-9962 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHenry Schein, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076887
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsTERBUTALINE SULFATE (1 mg/mL)
Marketing started20220112
Marketing ended20270301
Package count1

External sources

Source: openFDA. Public-domain (CC0).