CareCanon Independent health evidence
Menu
CareCanon directoryStart with the record you need.

Source-linked records · dates and limits kept visible

Source-linked dosage record

MOUNJARO dose chart

The Eli Lilly prescribing record for MOUNJARO (tirzepatide), organized into a scan-friendly schedule without detaching it from the source document.

Ingredient
tirzepatide
Schedule format
Label prose rendered as a table
Label published
May 06, 2026
Mirrored
2026-08-29
Source of record
FDA prescribing information for MOUNJARO, published May 06, 2026
setid d2d7da5d-ad07-4228-955f-cf7e355c8cc0mirrored

Answer first

Dose schedule

The source publishes the sequence in prose. CareCanon displays that rule as 6 inspectable rows.

WeeksDosagePhase
1 through 42.5 mgStarting dosage
5 through 85 mgDose escalation · label-named maintenance option
9 through 127.5 mgDose escalation · label-named maintenance option
13 through 1610 mgDose escalation · label-named maintenance option
17 through 2012.5 mgDose escalation · label-named maintenance option
21 and onward15 mgMaintenance dosage
How this schedule was produced

The manufacturer does not publish a titration table for MOUNJARO. The label states the escalation as a rule, quoted below, and the schedule above is that rule set out as a table. No dose has been added, and every dose shown appears in the label’s own “Dosage Forms and Strengths” section.

The recommended starting dosage is 2.5 mg injected subcutaneously once weekly. After 4 weeks, increase the dosage to 5 mg injected subcutaneously once weekly. If additional glycemic control is needed, increase the dosage in 2.5 mg increments after at least 4 weeks on the current dose.
: MOUNJARO prescribing information, section 2.1
Checked against label revision 12/2025.
MOUNJARO dose path chart with 6 source-linked schedule stages across 1 presentation
Visual index of the schedule above. It does not replace the table or source label.Open chart image ↗

Section 3 inventory

Strengths and presentations

This inventory is kept separate from the schedule: a marketed strength is not automatically a starting dose, maintenance dose or recommendation.

Marketed strengths in this brand record

  • 2.5 mg
  • 5 mg
  • 7.5 mg
  • 10 mg
  • 12.5 mg
  • 15 mg

Dosage forms

Injection

Named packages

  • Single-dose pen
  • Single-dose vial
  • Multi-dose vial · 4 doses
  • KwikPen · 4 doses

Source excerpt · 3 DOSAGE FORMS AND STRENGTHS

Injection: Clear, colorless to slightly yellow solution in pre-filled single-dose pens, single-dose vials, multi-dose vials, or single-patient-use KwikPens, each available in the following strengths. The multi-dose vials and single-patient-use KwikPen each contain 4 doses: Single-dose Pen or Vial 2.5 mg/0.5 mL 5 mg/0.5 mL 7.5 mg/0.5 mL 10 mg/0.5 mL 12.5 mg/0.5 mL 15 mg/0.5 mL Multi-dose Vial (4 doses per vial) Dose per Injection Total Strength per Total Volume Strength per mL 2.5 mg/0.6 mL 10 mg/2.4 mL 4.17 mg/mL 5 mg/0.6 mL 20 mg/2.4 mL 8.33 mg/mL 7.5 mg/0.6 mL 30 mg/2.4 mL 12.5 mg/mL 10 mg/0.6 mL 40 mg/2.4 mL 16.7 mg/mL 12.5 mg/0.6 mL 50 mg/2.4 mL 20.8 mg/mL 15 mg/0.6 mL 60 mg/2.4 mL 25 mg/mL Single-Patient-Use KwikPen (4 doses per KwikPen) Dose per Injection Total Strength per Total Vol

Inspect the complete section on DailyMed ↗

Source excerpts

What the label says

These excerpts preserve the section names used by the source. Open DailyMed for the complete prescribing information.

2 DOSAGE AND ADMINISTRATION

The recommended starting dosage is 2.5 mg injected subcutaneously once weekly. ( 2.1 ) After 4 weeks, increase to 5 mg injected subcutaneously once weekly. ( 2.1 ) If additional glycemic control is needed, increase the dosage in 2.5 mg increments after at least 4 weeks on the current dose. ( 2.1 ) Maximum dosage ( 2.1 ): Adults: 15 mg subcutaneously once weekly. Pediatric patients 10 years of age and older: 10 mg subcutaneously once weekly. Administer once weekly at any time of day, with or without meals. ( 2.2 ) Inject subcutaneously in the abdomen, thigh, or another person should inject in t

2.1 Recommended Dosage

The recommended starting dosage of MOUNJARO is 2.5 mg injected subcutaneously once weekly [see Dosage and Administration ( 2.2 )] . Follow the dosage escalation below to reduce the risk of gastrointestinal adverse reactions [see Warnings and Precautions ( 5.6 ) and Adverse Reactions ( 6.1 )] . The 2.5 mg dosage is for treatment initiation and is not intended for glycemic control. After 4 weeks, increase the dosage to 5 mg injected subcutaneously once weekly. If additional glycemic control is needed, increase the dosage in 2.5 mg increments after at least 4 weeks on the current dose. The maximu

2.2 Important Administration Instructions

Inform patients and their caregiver(s) which MOUNJARO presentation (e.g., vial, pre-filled single-dose pen, single-patient-use KwikPen) they will receive and ensure they receive training appropriate for that specific presentation. If the prescribed MOUNJARO presentation changes, ensure patients and caregivers receive appropriate training and instruct them to consult the Instructions for Use for the newly prescribed presentation. Prior to initiation, train patients and their caregiver(s) on proper injection technique for the prescribed MOUNJARO presentation [see Instructions for Use] . After tr

Document history

Recent label changes

Only changes named in the label’s own recent-major-changes block appear here.

SectionChangeRevised
1Indications and Usage12/2025
2.1Recommended Dosage12/2025
2.2Important Administration Instructions01/2026
5.6Warnings and Precautions Severe Gastrointestinal Adverse Reactions12/2025
5.10Never Share a MOUNJARO KwikPen Between Patients01/2026
Open the complete label-change ledger →

Before using this record

Three useful distinctions

Is this a personal dosing recommendation?

No. It is a reference rendering of prescribing information. A licensed prescriber and pharmacist determine what applies to an individual.

Did the manufacturer publish this exact table?

No. The label states the schedule in prose; CareCanon keeps the source sentence beside the table it renders.

How can I tell whether the source changed?

Use the publication and mirror dates above, inspect the recent-change rows, and open the linked DailyMed record for the current complete document.