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Peptide approval and evidence checker

Enter a peptide or brand name. See the reviewed status, human evidence, and exact product limits in one place.

U.S. Food and Drug Administration (FDA) records and research summaries. Not a live FDA check, medical advice, or product verification.

Editorial review · United States

Teduglutide

Source review:

Read the full Teduglutide review

Approval and product status

Teduglutide is a 33-amino-acid GLP-2 analog. In the United States, Gattex (teduglutide) is FDA-approved for people age 1 and older who have short bowel syndrome and depend on fluids or nutrition given through a vein.

Gattex evidence applies to a specific monitored prescription product. Gattex is a labeled prescription product used with structured monitoring. Its evidence does not establish general gut healing or equivalence for compounded GLP-2 analogues.

This is the status described in the dated review. It is not a live FDA database check.

What was measured in people?

Health outcomes · Strong
Randomized trials support reduction in parenteral-support requirements for short bowel syndrome.
Body effects · Strong
Intestinal absorption, exposure, and product effects are characterized in the label and trials.

A change in a hormone or body signal does not by itself prove a health benefit.

Limits that matter

Not independently medically reviewed. This tool does not recommend treatment.

This monitored prescription therapy has serious risks, including possible acceleration of neoplastic growth. No dosing, reconstitution, or self-treatment guidance is provided.

Still unknown: The evidence does not establish broad treatment of leaky gut, inflammatory symptoms, wellness, or mucosal repair in people without the labeled syndrome.

This record cannot check a package, seller, batch, or personal treatment. It does not provide sport clearance.

Exact product records in this review

These are selected records, not every product or form. A route means how a product enters the body.

Gattex

Form
Powder and diluent for injection
Route
Subcutaneous
Use and limits
Short bowel syndrome with parenteral-support dependence in the adult and pediatric populations defined in the label.

Published label: 2025 label

Read the published Gattex FDA label (PDF)

What the research shows

Randomized trials found that some participants needed less fluid or nutrition through a vein. The product label defines required screening and ongoing monitoring.

Read all Teduglutide claims and their limits

Sources used in the full review

A source is not support for every claim. Use the claim links above or the full review to check what each source supports.

  1. GATTEX (teduglutide) prescribing information

    U.S. Food and Drug Administration · Drug label · 2025

    Source accessed

  2. Teduglutide reduces parenteral support in short bowel syndrome

    PubMed · Gastroenterology · Randomized trial · 2012

    Source accessed

  3. Teduglutide orphan drug designation and approval

    U.S. Food and Drug Administration · Regulatory · 2019

    Source accessed

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Dataset version 2026-09-11.1. This endpoint grants no additional reuse license. Keep the verdict, scope, evidence basis, review date, and source links together. Do not present a record as medical advice or medical review.

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What the peptide approval checker shows

One name. Separate questions.

Approval applies to an exact product and use. Research may cover a different form, group of people, or outcome.

This tool keeps those questions separate. There is no safety score or treatment ranking.

Learn what FDA approval covers

Sources you can check.

Results use this site’s existing reviews. They show source dates, product labels, study limits, and links to the original records.

No answer is generated for an unknown name. An index-only entry stays marked as an incomplete review.

Read the evidence standard

Coverage and review dates

33 reviewed records and 20 index-only names. This is not a complete list of peptides or approved medicines.

Record reviews range from July 23, 2026 to August 30, 2026. The tool does not recheck FDA records each time you search.

Source reviews by Anthony Treviso. Not independently medically reviewed. Use the current official record to check for later changes.

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