Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Eli Lilly and Company names for other drugs.
Recalls
- Apr 5, 2022 · Class II · Cardinal Health Inc.
TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions
Lots: Lot #: D484557A, Exp: 10/25/2023. - Aug 19, 2021 · Class II · Eli Lilly & Company
Labeling: Label error on declared strength - autoinjector devices labeled as 0.75 mg / 0.5 mL actually contain 1.5 mg / 0.5 mL of product.
Lots: Lot number: D396436C
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Dulaglutide: every company that makes it
- Form
- injection, solution, subcutaneous
- Strength
- 0.75 mg per 0.5 mL
- Approval
- BLA BLA125469
- On the market since
- Sep 18, 2014
- Package NDCs
0002-1433-010002-1433-610002-1433-80- Official label
- DailyMed (National Library of Medicine), updated Jun 16, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?