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Terbutaline Sulfate

NDC 63323-665 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameTERBUTALINE SULFATE
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076887
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsTERBUTALINE SULFATE (1 mg/mL)
Marketing started20110310
Package count1

External sources

Source: openFDA. Public-domain (CC0).