Not FDA Approved

retatrutide

Manufactured by Eli Lilly

First of its kind: Retatrutide is not yet FDA-approved. It cannot legally be prescribed or dispensed by any pharmacy in the United States. Vials sold online with research-use-only labels are unregulated. This entry tracks the science and timeline; see /retatrutide for the full guide.

Compounded — Consider FDA-Approved Brands

Compounded retatrutide is legally restricted as of 2025 after the FDA declared the shortage resolved. If you're currently using a compounded version, consider switching to an FDA-approved brand.

Retatrutide

Eli Lilly's next-generation triple-agonist (GLP-1 + GIP + glucagon) weight loss injection. In late Phase 3 trials. Phase 2 results showed 24.2% body weight reduction at 48 weeks. Expected FDA decision late 2026 to early 2027.

See Retatrutide savings and coverage →

Overview

FDA Status

Not FDA Approved

Route

subcutaneous injection

Dosing

Typical Dose Range

1mg - 12mg weekly (Phase 3 dose range)

Dosing is determined by your prescribing provider based on your individual needs. Most GLP-1 medications follow a gradual titration schedule, starting at a low dose and increasing over several weeks to reduce side effects.

Cost Breakdown

Branded (Retail)

N/A

Savings Program

N/A

Prices are estimates and may vary by pharmacy, location, and insurance coverage. Contact your provider for accurate pricing.

Common Side Effects

  • nausea
  • diarrhea
  • vomiting
  • constipation
  • decreased appetite
  • transient heart rate increase

This is not a complete list of side effects. Talk to your healthcare provider about what to expect and when to seek medical attention.

This site is for educational purposes only and is not medical advice. Always consult a healthcare provider before starting any medication. Full disclaimer

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