Synedica Laboratories

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Each booklet below is the full instruction leaflet supplied with the unit — the same text, with the printed pages replaced by a page you can search, zoom, and print.
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  • The full printed text

    Each booklet is the instruction leaflet supplied with the unit, word for word.

  • Search, zoom and print

    The printed pages are replaced by a page you can search, zoom, and print.

  • Revision stamp

    The print code and revision date match the ones on the paper booklet.

2 booklets published

Confirm that the product name and strength match your pack before following a booklet. Dosing differs between products.

Instruction Booklet

Synedica Retatrutide® 60mg pre-filled pen

Read in full before use

Instruction booklet for the Synedica Retatrutide® 60mg solution for injection in a pre-filled pen — dosing, administration, side effects, and storage.

Print code
9-5184-01-096-3
Revised
08/2026

Product information

Pen contents
60mg retatrutide in 3ml
Concentration
20 mg/ml
Selectable doses
2.5 / 5 / 7.5 / 10 mg
Full doses per pen
6 × 10mg (0.5ml each)
Needles
Not included. Standard pen needles, 32G (0.23mm) × 4mm
Route
Subcutaneous, once weekly
Store unopened
2°C to 8°C, do not freeze
In use
6 weeks below 30°C

Contents of the leaflet

  1. 1What a Synedica Retatrutide® 60mg pen is and what it is used for
  2. 2What you need to know before using your Synedica Retatrutide® 60mg pen
  3. 3How to use Synedica Retatrutide® 60mg
  4. 4Possible side effects
  5. 5How to store Synedica Retatrutide®
  6. 6Contents of the pack and other information
Open the booklet →Formulation record

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.