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Comparison

Trulicity vs Ozempic

Trulicity

DULAGLUTIDE

Approved forType 2 diabetes, and cardiovascular risk in heart disease

Not weight loss

Eli Lilly and CompanyLabel version 62, effective 16 June 2026

Ozempic injection

SEMAGLUTIDE

Approved forType 2 diabetes, with cardiovascular and kidney indications

Not weight loss

A-S Medication SolutionsLabel version 1, effective 30 July 2026

Each stripe is one section of the label, each division in a stripe one entry in that section. The red bar marks a boxed warning.

Reference information, not medical advice

This page is a reference, not medical advice. It reports what the FDA-approved label states and links to that label. It does not tell anyone what to take, and it cannot replace a conversation with a doctor or pharmacist who knows the person's history.

Trulicity and Ozempic are the two best known weekly injections in the GLP-1 class, and they contain different molecules. Both labels cover type 2 diabetes. Neither covers weight management, which is the use most people are asking about when they compare them.

01

Side by side, straight from the labels

From the FDA label

This table is generated from the two source labels, not typed out by hand, so it cannot drift from what the regulator approved.

Label sectionTrulicityDULAGLUTIDEOzempic injectionSEMAGLUTIDE
Active ingredientDulaglutideGLP-1 receptor agonistSemaglutideGLP-1 receptor agonist
Approved forType 2 diabetes, and cardiovascular risk in heart diseaseType 2 diabetes, with cardiovascular and kidney indications
SupplyPrescriptionPrescription
What pharmacies payAcquisition cost, not retail$487.63 per millilitre, brand$331.98 per millilitre, brand
Boxed warningWARNING: RISK OF THYROID C-CELL TUMORSWARNING: RISK OF THYROID C-CELL TUMORS
What the FDA approved it for
  • To reduce the risk of major adverse cardiovascular events (cardiovascular death, non-fatal myocardial infarction, or non-fatal stroke) in adults with type 2 diabetes mellitus who have established cardiovascular disease or multiple cardiovascular risk factors.
  • TRULICITY ® is a glucagon-like peptide-1 (GLP-1) receptor agonist indicated: As an adjunct to diet and exercise to improve glycemic control in adults and pediatric patients 10 years of age and older with type 2 diabetes mellitus.
  • as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
  • to reduce the risk of major adverse cardiovascular events in adults with type 2 diabetes mellitus and established cardiovascular disease.
  • to reduce the risk of sustained eGFR decline, end-stage kidney disease and cardiovascular death in adults with type 2 diabetes mellitus and chronic kidney disease.
Forms and strengths
  • Injection: TRULICITY is a clear and colorless solution available as: 0.75 mg/0.5 mL solution in a single-dose pen 1.5 mg/0.5 mL solution in a single-dose pen 3 mg/0.5 mL solution in a single-dose pen...
  • Injection: 2 mg/3 mL (0.68 mg/mL) for 4 doses of 0.25 mg and 2 doses of 0.5 mg or 4 doses of 0.5 mg, 4 mg/3 mL (1.34 mg/mL) for 4 doses of 1 mg, and 8 mg/3 mL (2.68 mg/mL) for 4 doses of 2 mg in...
  • Injection: 0.25 mg, 0.5 mg or 1 mg per 0.5 mL in a single-dose prefilled syringe
How the label says it is taken
  • Recommended starting dosage is 0.75 mg injected subcutaneously once weekly. After 4 weeks, the dosage may be increased to 1.5 mg once weekly for additional glycemic control. If additional glycemic control is needed, increase dosage in 1.5 mg increments after at least 4 weeks on the current dosage. Maximum recommended dosage is 4.5 mg injected subcutaneously once weekly. Pediatric Dosage
  • If a dose is missed, administer the missed dose as soon as possible if there are at least 3 days (72 hours) until the next scheduled dose. Important Administration Instructions
  • Administer once weekly at any time of day with or without food. Inject subcutaneously in the abdomen, thigh, or upper arm.
  • Administer once weekly at any time of day, with or without meals.
  • Start at 0.25 mg once weekly. After 4 weeks, increase the dosage to 0.5 mg once weekly.
  • If additional glycemic control is needed, increase the dosage to 1 mg once weekly after at least 4 weeks on the 0.5 mg dose.
  • To reduce the risk of sustained eGFR decline, end-stage kidney disease and cardiovascular death, increase the dosage to 1 mg once weekly after at least 4 weeks on the 0.5 mg dosage.
  • If a dose is missed, administer within 5 days of missed dose.
  • Inject subcutaneously in the abdomen, thigh, or upper arm. Important Administration Instructions
Most common adverse reactions
  • Most common adverse reactions (incidence ≥5%) are nausea, diarrhea, vomiting, abdominal pain, and decreased appetite.
  • most common adverse reactions reported in ≥5% of patients treated with OZEMPIC are: nausea, vomiting, diarrhea, abdominal pain and constipation.
Warnings and precautions
  • Thyroid C-cell Tumors: See Boxed Warning.
  • Acute Pancreatitis: Has been observed in patients treated with GLP-1 receptor agonists, including TRULICITY.
  • Discontinue if pancreatitis is suspected.
  • Hypoglycemia: Concomitant use with an insulin secretagogue or insulin may increase the risk of hypoglycemia, including severe hypoglycemia.
  • Acute Pancreatitis: Has been observed in patients treated with GLP-1 receptor agonists, including OZEMPIC. Discontinue if pancreatitis is suspected.
  • Diabetic Retinopathy Complications: Has been reported in a clinical trial. Patients with a history of diabetic retinopathy should be monitored.
  • Never share an OZEMPIC pen between patients, even if the needle is changed.
  • Hypoglycemia: Concomitant use with an insulin secretagogue or insulin may increase the risk of hypoglycemia, including severe hypoglycemia. Reducing dose of insulin secretagogue or insulin may be necessary.
  • Acute Kidney Injury Due to Volume Depletion: Monitor renal function in patients reporting adverse reactions that could lead to volume depletion.
  • Severe Gastrointestinal Adverse Reactions: Use has been associated with gastrointestinal adverse reactions, sometimes severe. OZEMPIC is not recommended in patients with severe gastroparesis.
  • Hypersensitivity Reactions: Serious hypersensitivity reactions (e.g., anaphylaxis and angioedema) have been reported. Discontinue OZEMPIC if suspected and promptly seek medical advice.
  • Acute Gallbladder Disease: If cholelithiasis or cholecystitis are suspected, gallbladder studies are indicated.
Contraindications
  • TRULICITY is contraindicated in patients with: Personal or family history of medullary thyroid carcinoma (MTC) or in patients with Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).
  • Serious hypersensitivity reaction to dulaglutide or to any of the product components.
  • Serious hypersensitivity reactions including anaphylactic reactions and angioedema have been reported with TRULICITY.
  • Personal or family history of MTC or in patients with MEN 2.
  • Serious hypersensitivity reaction to semaglutide or any of the excipients in OZEMPIC.
Drug interactions
  • Oral Medications: Delays gastric emptying and has the potential to reduce the rate of absorption of concomitantly administered oral medications.
  • Oral Medications: OZEMPIC delays gastric emptying.
  • May impact absorption of concomitantly administered oral medications.
  • Use with caution.
Label version16 June 202630 July 2026

Comparison of Trulicity vs Ozempic taken from the FDA labels.

02

Neither label approves weight loss, and the reason differs

Written by us

The Trulicity label covers glycaemic control in type 2 diabetes in adults and paediatric patients aged 10 and older, and reducing the risk of major adverse cardiovascular events in adults who have type 2 diabetes with established cardiovascular disease or multiple risk factors. The Ozempic label covers glycaemic control in adults, the same cardiovascular indication in adults with established disease, and a third indication for kidney outcomes in chronic kidney disease.

Semaglutide does hold a weight management approval in the United States, under the separate name Wegovy. Dulaglutide holds no such approval at all: there is no second brand, no second label, and nothing in the approved document that describes it for weight.

03

Same class, and the boxed warning is the same

Written by us

Both carry the boxed warning about the risk of thyroid C-cell tumours observed in rodents, and both are contraindicated in anyone with a personal or family history of medullary thyroid carcinoma or with multiple endocrine neoplasia syndrome type 2. Repeated word for word across products of one class, that is a class warning rather than a statement about either product.

Below the box the lists run close: acute pancreatitis, hypoglycaemia when combined with insulin or an insulin secretagogue, kidney injury, serious hypersensitivity. The Ozempic label adds diabetic retinopathy complications and an instruction that a pen must never be shared between patients.

04

Dosing is where the two documents actually diverge

Written by us

Trulicity starts at 0.75 mg once weekly, may go to 1.5 mg after four weeks, and can be escalated further; it is supplied in single-dose pens of 0.75 mg, 1.5 mg, 3 mg and 4.5 mg. Ozempic starts at 0.25 mg once weekly, moves to 0.5 mg after four weeks, and can go to 1 mg and then 2 mg.

The numbers are not comparable between products: milligrams of dulaglutide and milligrams of semaglutide are different substances, and neither label converts one into the other.

A missed dose is handled differently, and this is a practical difference rather than a pharmacological one. Trulicity may be taken as soon as possible if at least 72 hours remain before the next scheduled dose. Ozempic may be taken within 5 days of the missed dose.

05

The reported common reactions are close but not identical

Written by us

Both labels use a 5 percent threshold. Trulicity lists nausea, diarrhoea, vomiting, abdominal pain and decreased appetite. Ozempic lists nausea, vomiting, diarrhoea, abdominal pain and constipation.

The difference is at the end of each list: decreased appetite appears for one, constipation for the other. Both lists come from separate trials in different populations, so this is not a measured difference between the two products.

06

One is a biologic, the other is not

Written by us

Trulicity is approved under a biologics licence application rather than a new drug application, because dulaglutide is a protein. That is why there is no generic dulaglutide and will not be one: copies of biologics reach the market as biosimilars, under their own approvals.

Semaglutide is approved under a new drug application. Neither route says anything about how well either medication works; it determines what a copy of it would have to be called and how it would be approved.

07

Common questions

Written by us
Is Trulicity or Ozempic approved for weight loss?
Neither. Both labels cover type 2 diabetes, with cardiovascular indications alongside. Semaglutide holds a separate weight management approval under the name Wegovy; dulaglutide holds no weight approval under any name.
Which one is stronger?
The labels do not compare them, and their doses cannot be compared either: 4.5 mg of dulaglutide and 2 mg of semaglutide are amounts of different substances. This page does not rank them.
What happens if a weekly dose is missed?
The two labels answer differently. Trulicity may be given as soon as possible provided at least 72 hours remain until the next scheduled dose. Ozempic may be given within 5 days of the missed dose. After those windows both labels direct the patient to skip and resume the usual schedule.
Is there a generic version of either?
Not for dulaglutide: it is a biologic, so copies would be biosimilars rather than generics, and none is approved. Semaglutide is a small molecule approved under a new drug application, but no approved generic semaglutide exists in the United States either.
08

Sources

Every fact above comes from one of these documents. The date is the effective date of the label version this page was built from.

Other comparisons in this category

Page last updated: 14 August 2026

Compiled by the HealthyStudy editorial team from FDA source documents. No medical reviewer is credited on this page, because none reviewed it.