# Trulicity

NDC: 0002-3182
Generic name: Dulaglutide
Labeler / Manufacturer: Eli Lilly and Company
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: INJECTION, SOLUTION
Routes: SUBCUTANEOUS
Marketing started: 20200903

FDA application: BLA125469

## Active ingredients

- DULAGLUTIDE: 4.5 mg/.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0002-3182"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0002-3182
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=463050bd-2b1c-40f5-b3c3-0a04bb433309