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Retatrutide 40mg Injection Pen Kit

Retatrutide 40mg Injection Pen Kit

Retatrutide 40mg in a pen-format unit.

Active ingredient
Retatrutide
Strength
40mg
Format
Injection pen
CertificateSYN-COA-2026-RET040-2106Batch SYN-RET040-2106

For research reference only. Check the linked batch and lab documents before relying on a unit.

Specification

Active Ingredient
Retatrutide
Nominal Amount
40mg
Format
Injection pen
Category
Metabolic

Presentation and contents

  • 1× pen-format unit (40mg)
  • 12× disposable 32G 4mm needles
  • documentation insert

Mechanism

Receptors and pathways

Retatrutide

Targets

  • GIP receptor
  • GLP-1 receptor
  • Glucagon receptor

A single peptide agonist of the GIP, GLP-1 and glucagon receptors.

Reference data

Molecular weight
4769.5 Da
Reported half-life
~6 days

Reference values for the molecule from the Synedica library. They were not measured on this batch.

Lab testing

Results on the current certificate

Passed
15/15
Testing laboratory
Synedica Analytical Laboratories
Current batch
SYN-RET040-2106

Identity and description

Confirms the substance and its appearance match the specification.

2/2
  • Appearance

    Visual inspection, Ph. Eur. 2.2.1

    SpecificationClear, colourless solution, free from visible particles

    ResultConforms

    Pass
  • Identity

    ESI-MS, ≤ 5 ppm

    SpecificationConfirmed [M+5H]⁵⁺ = 947.3

    ResultConfirmed

    Pass

Strength and purity

How much active ingredient is present, and how much of it is the intended compound.

3/3
  • Assay (content)

    RP-HPLC-UV, C18, 220 nm

    Specification95.0 – 105.0% of label claim

    Result101.9%

    Pass
  • Purity

    RP-HPLC-UV, C18, 220 nm

    Specification≥ 98.0%

    Result99.0%

    Pass
  • Related substances

    RP-HPLC-UV, area normalisation

    Specification≤ 2.0% total

    Result1.0%

    Pass

Safety and contaminants

Microbial, endotoxin, particle and elemental impurity limits.

5/5
  • Visible particles

    Ph. Eur. 2.9.20

    SpecificationPractically free from visible particles

    ResultConforms

    Pass
  • Particulate matter (sub-visible)

    Light obscuration, Ph. Eur. 2.9.19

    SpecificationMeets Ph. Eur. limits for parenteral use

    ResultConforms

    Pass
  • Sterility

    Membrane filtration, Ph. Eur. 2.6.1

    SpecificationNo growth at 14 days

    ResultConforms

    Pass
  • Bacterial endotoxins

    LAL kinetic chromogenic, Ph. Eur. 2.6.14

    Specification< 10.0 EU/mL

    Result< 0.13 EU/mL

    Pass
  • Elemental impurities

    ICP-MS, ICH Q3D / Ph. Eur. 2.4.20

    SpecificationMeets ICH Q3D parenteral limits

    ResultConforms

    Pass

Solution and container

Physical properties of the solution and the integrity of its container.

5/5
  • pH

    Potentiometry, Ph. Eur. 2.2.3

    Specification7.0 – 8.0

    Result7.20

    Pass
  • Osmolality

    Ph. Eur. 2.2.35

    Specification270 – 330 mOsm/kg

    Result285 mOsm/kg

    Pass
  • Preservative content

    RP-HPLC-UV (m-cresol)

    Specification85.0 – 115.0% of label claim

    Result95.1%

    Pass
  • Extractable volume

    Ph. Eur. 2.9.17

    Specification≥ label claim

    ResultConforms

    Pass
  • Container closure integrity

    Dye ingress, ASTM F1929

    SpecificationNo ingress

    ResultConforms

    Pass
PassSYN-COA-2026-RET040-2106Issued 2026-07-13

Traceability

From batch to your unit

  1. 01

    Batch produced

    SYN-RET040-2106

  2. 02

    Laboratory analysis

    Synedica Analytical Laboratories

    15 tests

  3. 03

    Certificate issued

    SYN-COA-2026-RET040-2106

    2026-07-13

  4. 04

    Unit code printed

    One code per unit

  5. 05

    You verify

    Enter the code on this page

Packaging security

Verify this unit

Unit code

Reta Pen 40mg

The 6-character code is under the scratch-off panel on the pack.

Check the pack before you open it

A genuine pack carries a holographic seal, a tamper seal and a scratch-off panel over the unit QR code and its 6-character code.

What a genuine pack carriesLOTEXPINSIDE THE BOX
  1. Holographic seal
  2. Tamper seal
  3. Scratch-off panel
  4. Information QR code
  5. Batch number and expiry date
  6. Product name and strength
Schematic drawing. The position of each feature differs between products.
How falsified packs are recognised

Questions about this formulation

How does it differ from the Reta Pen 60mg?

The 60mg pen holds 60mg in 3ml and has a published instruction booklet. The fill volume of the 40mg pen is not published yet.

Is this formulation for use in people?

No. Synedica formulations are supplied for laboratory research use only.

How do I check that a pack is genuine?

Check that the holographic seal and the tamper seal are intact. Then scratch off the panel and scan the unit QR code, or enter its 6-character code in the form on this page.

Where is the certificate for my batch?

Certificates are listed by batch number in the certificate register. Match it to the batch number printed on your pack.

Research Use Only

Material referenced on this site is supplied for laboratory and analytical research use only. It is not a drug, biologic, medical device, dietary supplement, or cosmetic, is not intended for human or veterinary use, and has not been evaluated by the U.S. Food and Drug Administration. Nothing on this site is medical advice or a recommendation to diagnose, treat, cure, or prevent any condition. Visitors are solely responsible for determining and complying with the laws applicable to research material in their jurisdiction.

Reta Pen 40mg

Verify this unit