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Sandostatin

NDC 0078-0182 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameoctreotide acetate
Labeler / ManufacturerNovartis Pharmaceuticals Corporation
Marketing categoryNew Drug Application (innovator) · App NDA019667
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsOCTREOTIDE ACETATE (500 ug/mL)
Marketing started19881021
Package count1

External sources

Source: openFDA. Public-domain (CC0).