FDA NDC Directory · JSON-LD · Markdown

Gattex

NDC 68875-0101 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameteduglutide
Labeler / ManufacturerTakeda Pharmaceuticals America, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA203441
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · SUBCUTANEOUS
Active ingredientsTEDUGLUTIDE (5 mg/.5mL)
Marketing started20121221
Package count1

External sources

Source: openFDA. Public-domain (CC0).