FDA NDC Directory · JSON-LD · Markdown

Trulicity

NDC 0002-2236 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameDulaglutide
Labeler / ManufacturerEli Lilly and Company
Marketing categoryBiologic License Application · App BLA125469
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsDULAGLUTIDE (3 mg/.5mL)
Marketing started20200903
Package count2

External sources

Source: openFDA. Public-domain (CC0).