Peptide Legal Status

Look up the current FDA regulatory status and legal access classification for research peptides and compounds.

Data last verified: April 13, 2026

Regulatory status data reflects information available as of the date shown. Verify current status through official FDA channels.

Showing 30 of 30 compounds

5-Amino-1MQ

Class
Small molecule
FDA
Not FDA approved
Access
Research chemical
Summary
5-Amino-1MQ is a quinolinone derivative studied in nicotinamide N-methyltransferase–related metabolic models; it is not FDA-approved as a marketed drug product.

AOD-9604

Anti-Obesity Drug 9604

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
AOD-9604 is a modified fragment of human growth hormone studied in metabolic and lipolysis-related research. U.S. regulatory treatment remains in flux after a February 2026 HHS announcement; formal FDA guidance reflecting that announcement had not been issued as of April 2026.

BPC-157

Body Protection Compound-157

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
BPC-157 is a synthetic peptide sequence studied in laboratory and preclinical research models. U.S. regulatory treatment remains in flux after a February 2026 HHS announcement; formal FDA guidance reflecting that announcement had not been issued as of April 2026.

CJC-1295

CJC-1295 DAC, Mod GRF 1-29

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
CJC-1295 refers to modified growth hormone–releasing hormone analog peptides studied in laboratory research. U.S. regulatory treatment remains in flux after a February 2026 HHS announcement; formal FDA guidance reflecting that announcement had not been issued as of April 2026.

Dihexa

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
Dihexa is an oligopeptide-derived compound studied in synaptic plasticity and cognitive preclinical models; it is not FDA-approved as a marketed drug product.

DSIP

Delta sleep-inducing peptide

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
DSIP is a neuropeptide studied in sleep physiology and stress-related laboratory models; it is not FDA-approved as a marketed drug product.

Epithalon

Epitalon

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
Epithalon (epitalon) is a synthetic tetrapeptide studied in aging-related laboratory models; it is not FDA-approved as a marketed drug product.

GHK-Cu

Copper peptide GHK

Class
Peptide
FDA
Not FDA approved
Access
Research chemical (injectable), OTC (topical)
Summary
GHK-Cu is a copper-complexed tripeptide used in cosmetic peptide research and related topical formulation categories, and it appears in non-cosmetic research contexts as well. U.S. regulatory framing can differ by route; formal FDA guidance following the February 2026 HHS announcement had not been published as of April 2026.

Gonadorelin

Factrel, GnRH

Approved in multiple countries including the US, EU, and UK.

Class
Peptide
FDA
FDA approved
Access
Prescription
Summary
Gonadorelin (GnRH) is a decapeptide hypothalamic hormone used in FDA-approved diagnostic testing contexts for pituitary function, available by prescription.

Humanin

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
Humanin is a mitochondrial-derived peptide studied in cell stress, metabolism, and aging-related laboratory models; it is not FDA-approved as a marketed drug product.

Ipamorelin

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
Ipamorelin is a growth hormone secretagogue-related pentapeptide studied in laboratory research. U.S. regulatory treatment remains in flux after a February 2026 HHS announcement; formal FDA guidance reflecting that announcement had not been issued as of April 2026.

Kisspeptin-10

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
Kisspeptin-10 is a kisspeptin fragment studied in reproductive neuroendocrine research; it is not FDA-approved as a marketed drug product.

KPV

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
KPV is a tripeptide fragment studied in anti-inflammatory and barrier-related laboratory models. U.S. regulatory treatment remains in flux after a February 2026 HHS announcement; formal FDA guidance reflecting that announcement had not been issued as of April 2026.

LL-37

Cathelicidin

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
LL-37 is the human cathelicidin antimicrobial peptide studied in innate immunity and infection-related research; it is not FDA-approved as a marketed drug product.

Melanotan II

MT-2

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
Melanotan II is a synthetic cyclic melanocortin peptide studied in laboratory models related to pigmentation biology; it is not FDA-approved as a marketed drug product.

MK-677

Ibutamoren

Class
Small molecule
FDA
Not FDA approved
Access
Research chemical
Summary
MK-677 (ibutamoren) is an orally active ghrelin receptor agonist studied as a growth hormone secretagogue in clinical pharmacology research; it is not FDA-approved as a marketed drug product.

MOTS-c

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
MOTS-c is a mitochondrial open reading frame–associated peptide studied in metabolic regulation and exercise biology models. U.S. regulatory treatment remains in flux after a February 2026 HHS announcement; formal FDA guidance reflecting that announcement had not been issued as of April 2026.

NAD+

Nicotinamide adenine dinucleotide

Class
Small molecule
FDA
Not FDA approved
Access
OTC supplement category for certain precursors (for example NMN and NR marketed as dietary ingredients); IV infusion use appears in clinic settings outside a unified FDA drug product pathway.
Summary
NAD+ (nicotinamide adenine dinucleotide) is a ubiquitous redox coenzyme studied in cellular energetics and aging-related biology. It is not FDA-approved as a drug in the way small-molecule medicines are typically reviewed, while related precursors are commonly sold as dietary supplements and some clinics offer IV formulations outside a single standardized approval framework.

Oxytocin

Pitocin

Listed on the WHO Essential Medicines List; widely approved globally.

Class
Peptide
FDA
FDA approved
Access
Prescription
Summary
Oxytocin is a nonapeptide hormone used as an FDA-approved drug for specific obstetric indications when manufactured and labeled as a drug product, available by prescription.

PT-141

Bremelanotide, Vyleesi

Approved in the US only.

Class
Peptide
FDA
FDA approved
Access
Prescription
Summary
PT-141 (bremelanotide) is a cyclic peptide melanocortin receptor agonist approved as a drug product for a specific indication and available by prescription.

Retatrutide

LY3437943

Investigational globally (Phase 3).

Class
Peptide
FDA
Investigational
Access
Not yet available
Summary
Retatrutide is a triple incretin agonist peptide in late-stage clinical development for obesity and related metabolic endpoints; it is not FDA-approved or generally available as a commercial drug product as of April 2026.

Selank

Approved in Russia as an anxiolytic.

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
Selank is a synthetic heptapeptide studied in anxiety- and cognition-related research, including approvals outside the United States. U.S. regulatory treatment remains unsettled; formal FDA guidance following the February 2026 HHS announcement had not been published as of April 2026.

Semaglutide

Ozempic, Wegovy, Rybelsus

Approved in EU (EMA), Japan, UK, Canada, Australia, and 80+ other countries.

Class
Peptide
FDA
FDA approved
Access
Prescription
Summary
Semaglutide is a GLP-1 receptor agonist available in injectable and oral dosage forms under FDA-approved indications for type 2 diabetes and chronic weight management, available by prescription.

Semax

Approved in Russia and Ukraine for cognitive and neurological indications.

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
Semax is a synthetic heptapeptide studied in cognitive and neurological research, including approvals outside the United States. U.S. regulatory treatment remains unsettled; formal FDA guidance following the February 2026 HHS announcement had not been published as of April 2026.

Sermorelin

Geref

Previously approved in the US only; not marketed internationally.

Class
Peptide
FDA
Previously approved
Access
Compounding pharmacy (prescription)
Summary
Sermorelin acetate is a growth hormone–releasing hormone (1–29) analog that was previously FDA-approved and later withdrawn by the sponsor; regulatory discussions note that prior approval history can influence how it is treated in pharmacy compounding contexts compared with peptides lacking an approval history.

SS-31

Elamipretide

Investigational globally.

Class
Peptide
FDA
Investigational
Access
Not yet available
Summary
SS-31 (elamipretide) is a mitochondria-targeted tetrapeptide studied in primary mitochondrial disease trials; it is not FDA-approved for broad marketing as of April 2026.

TB-500

Thymosin Beta-4 fragment

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
TB-500 commonly denotes a thymosin beta-4–related peptide fragment studied in tissue repair and cell migration preclinical models. U.S. regulatory treatment remains in flux after a February 2026 HHS announcement; formal FDA guidance reflecting that announcement had not been issued as of April 2026.

Tesamorelin

Egrifta

Approved in the US and Canada.

Class
Peptide
FDA
FDA approved
Access
Prescription
Summary
Tesamorelin is a growth hormone–releasing factor analog approved for excess abdominal fat in HIV-associated lipodystrophy, available by prescription under FDA-labeled indications.

Thymosin Alpha-1

Ta1, Zadaxin

Not FDA-approved as a drug; approved in 35+ countries (e.g. China, Russia, India, Philippines) as Zadaxin for hepatitis B/C and as an immune adjuvant.

Class
Peptide
FDA
Not FDA approved
Access
Research chemical
Summary
Thymosin alpha-1 is a thymic peptide studied in immunology and vaccine adjuvant research and is approved in many countries outside the United States. U.S. regulatory treatment remains in flux after a February 2026 HHS announcement; formal FDA guidance reflecting that announcement had not been issued as of April 2026.

Tirzepatide

Mounjaro, Zepbound

Approved in EU (EMA), Japan, UK, and 30+ other countries.

Class
Peptide
FDA
FDA approved
Access
Prescription
Summary
Tirzepatide is an injectable dual glucose-dependent insulinotropic polypeptide and GLP-1 receptor agonist studied and marketed for glycemic control and weight management under FDA-approved indications, available by prescription.