Major regulatory hurdles cleared. Dispensing expected October 2026.
BPC-157, TB-500, KPV, MOTS-C, and Semax have cleared the primary FDA regulatory hurdles. Formal dispensing authorisation is expected around October 2026. WellSpry will begin prescribing these immediately upon availability — test now so your baseline is ready.
BPC-157
TB-500
KPV
MOTS-C
Semax
Announced for reclassification February 27, 2026. Formal Federal Register publication not yet issued. WellSpry monitors the Federal Register daily.
AOD-9604
Emideltide (DSIP)
Epitalon
GHK-Cu Injectable
Kisspeptin-10
Thymosin Alpha-1
The next wave. FDA review scheduled for February 2027.
LL-37, GHK-Cu, Dihexa acetate, Melanotan II, and PEG-MGF are lined up for formal FDA review by February 2027. Each has a distinct clinical application — antimicrobial defence, collagen repair, neural synaptogenesis, melanocortin signalling, and satellite cell activation. Test now to have your baseline documented before prescribing opens.
LL-37
GHK-Cu
Dihexa Acetate
Melanotan II
PEG-MGF
Beyond peptides — protocols that work alongside them.
WellSpry integrates NAD+ and other evidence-based longevity protocols with biomarker-driven prescribing. Every protocol is physician-ordered and monitored by lab results.
NAD+
WellSpry peptide prescribing
Your 100+ biomarker panel and gut score create the clinical documentation.
Your physician reviews the results and identifies which peptides are warranted — if any.
Patient-specific prescription sent to our 503A licensed pharmacy network (Belmar Pharma).
You fill the prescription directly. WellSpry never touches the compound.
This is not a questionnaire. This is not a research chemical vendor. This is a board-certified physician reading your actual biomarkers and writing a patient-specific prescription through a licensed 503A compounding pharmacy. Biomarker-driven. Physician-authorised. Fully documented.