503A Peptide and NAD+ Formulary for Prescribing Practices
This formulary is for licensed prescribers. ExaVeyra refers practices to its 503A pharmacy partner, which dispenses NAD+, glutathione and other compounded preparations on a patient-specific prescription in the states it is licensed to ship into. Each preparation's supplier documentation is reviewed by an organic chemist, and a certificate of analysis is available on request. Practices can apply or ask a question without an NPI; verification unlocks the full formulary with strengths, fills and beyond-use dates.
Browse by category
- Compounded Hormone FormulationsBi-Est, estradiol, progesterone, DHEA, T4/T3 and low dose naltrexone, compounded to prescriber-specified strengths in capsule and cream.9 compounds · 54 formulations · 180 days to Per prescription beyond-use dates
- Injectable Vitamins and IV SolutionsNAD+, glutathione, ascorbic acid, methylcobalamin and B-complex compounded for injectable and IV administration.9 compounds · 14 formulations · 30 days to 90 days beyond-use dates
- Topical and Cosmeceutical FormulationsGHK-Cu, SNAP-8, niacinamide and methylene blue topicals compounded in 30 g creams and 30 mL serums.7 compounds · 7 formulations · 180 days beyond-use date
- Hair and Scalp FormulationsMinoxidil combinations, topical finasteride and GHK-Cu scalp solutions compounded in 30 and 60 mL solutions.4 compounds · 4 formulations · 180 days to 35 days beyond-use dates
- Topical Anesthetic FormulationsBenzocaine, lidocaine, tetracaine and prilocaine combinations in 60 mL pumps, compounded against an individual prescription.5 compounds · 5 formulations · 180 days beyond-use date
Every 503A Compound, One Searchable Library
Filter by therapeutic group or search by name, mechanism, or research area. Each compound has a dedicated page ready for peer-reviewed enrichment.
The shipped catalog is not the whole formulary
The compounding partner maintains a broader 503A formulary with per-unit pricing, restricted to licensed healthcare providers. Verified practices can request access.
Practitioner Reserve Collection
Beyond the public library, approved practices see a reserve of compounded formulations with full specifications, beyond-use dates and lot documentation, inside the practitioner portal.
The collection opens in your practitioner portal once your NPI and license are verified and our team approves your practice. Compounded preparations are dispensed by our 503A pharmacy partner on a patient-specific prescription.
What Are Bioactive Small Molecules?
Bioactive small molecules are low-molecular-weight compounds that interact directly with biological systems at the cellular and subcellular level. Unlike large biologics such as proteins or antibodies, small molecules can cross cell membranes and engage intracellular targets, making them powerful tools for modulating cellular energy, redox balance, and metabolic function.
In regenerative and longevity medicine, small molecules like NAD+ precursors, coenzymes, and antioxidant tripeptides are widely studied. Their mechanisms are well-characterized in the biochemical literature, and prescribers weigh the published evidence for each compound within their own clinical judgment.

ExaVeyra's small molecule catalog is curated by our founder, an M.Sc. organic chemist, who evaluates every product against its underlying chemistry, manufacturing methodology, and analytical data. We supply only formulations that meet our documentation and purity standards, compounded by a licensed 503A pharmacy against individual prescriptions.
Organic Chemist-Verified: Every small molecule in the ExaVeyra catalog is reviewed by our founder, Benn, an M.Sc. organic chemist with expertise in synthetic organic chemistry, analytical chemistry, and biochemistry. We go beyond COA review to evaluate the chemistry itself.
Practices We Supply
Licensed practices order these formulations for protocols their own prescribers design. We provide the formulation and its lot documentation.
Longevity and Wellness Practices
NAD+ and glutathione, compounded against an individual prescription, with the certificate of analysis for every lot.
IV Therapy Practices
Injectable NAD+, glutathione, ascorbic acid and B vitamins in the vial sizes and concentrations the pharmacy lists.
Integrative Medicine Practices
Glutathione and ascorbic acid preparations, supplied with lot documentation for the prescriber's own protocol.
Aesthetic Practices
Topical formulations such as GHK-Cu, niacinamide and methylene blue creams and serums, compounded against an individual prescription.
Functional Medicine Practices
NAD+, methylcobalamin and B-complex preparations, each lot with its certificate of analysis and beyond-use date.
Licensed 503A Pharmacy, Chemist-Reviewed Documentation
All ExaVeyra small molecule formulations are prepared by a 503A pharmacy licensed by its state Board of Pharmacy, against a valid prescription for an individual patient. ExaVeyra does not work with a 503B outsourcing facility. A manufacturer certificate of analysis covering purity, potency, and sterility is available on request. Lot tracking is available for every batch to support your practice's compliance requirements.
Our sourcing process is reviewed by an M.Sc. organic chemist who evaluates the analytical methodology behind each preparation's release documentation, including HPLC, mass spectrometry and endotoxin testing.

503A Pharmacy Sourcing
Prepared by a 503A pharmacy licensed by its state Board of Pharmacy, with documented quality systems.
Release Documentation
The pharmacy documents purity, potency and, for sterile preparations, sterility results for each lot, and our chemist reviews the methods behind them.
Beyond-Use Dating
Each preparation carries the pharmacy's beyond-use date, set from stability data for that formulation and printed on its label.
Research summaries are provided for educational purposes. Connect with our compliance team before integrating any protocol.
Speak With Our Compliance Team
Our team can walk you through research context, sourcing questions, and regulatory considerations. Select any areas of interest and we'll connect you with the right specialist.
Areas of Interest Check all that apply
All inquiries are reviewed by our compliance and research team. We do not share your information with third parties.
Small Molecule Products
The formulary and pricing are released after NPI verification and a review of your practice.
Supply and documentation
- Lead time
- 3 to 5 business days from order to delivery, covering both preparation and transit.
- Coverage
- licensed in 33+ states, with licensure confirmed for your destination before a first order ships
- Testing
- Endotoxin and sterility testing on every sterile batch
- Compounded under USP General Chapters 795, 797 and 800
- Compounded by a 503A pharmacy licensed by its state Board of Pharmacy, against a prescription for an individual patient
- Lot identification and the assigned beyond-use date on every container label
- Certificates of Analysis are documented and lot-specific, held on file with the pharmacy for your records.
- Account review in 1 to 3 business days for licensed clinics and practitioners
- Same-day quotes
- Orders placed with the pharmacy within 24 hours of approval
- A dedicated account manager for each practice
ExaVeyra exists to simplify access to biologics, molecules and medical devices through one point of contact, so a practice runs one account rather than three.
- Every formulary page is checked by a chemist. ExaVeyra was founded by an M.Sc. organic chemist, and specification data is verified against the source catalog rather than reproduced from a vendor sheet.
- One verified account covers biologics, 503A compounded formulations and devices, with a single account manager rather than a separate vendor relationship for each.
Request the full formulary and pricing
The pages on this site list a representative selection. Verified practitioners receive the complete named formulary, current pricing, available strengths and formats, and the identity and credentials of the compounding pharmacy that prepares each preparation.
Access requires a valid NPI. Compounded formulations are prepared by our 503A pharmacy partner, a compounding pharmacy licensed by the Texas State Board of Pharmacy. We verify the number against the national registry, and our team reviews each practice before releasing the formulary, which is why pricing is not published openly: these are prescription preparations supplied to licensed practices rather than consumer products.
Already verified? Sign in to the provider portal
Compounded medications are not FDA-approved finished drug products. Preparations are dispensed against a prescription for a named patient. Nothing on this page is medical advice or a recommendation for any patient.
Ready to Add NAD+ & Glutathione to Your Practice?
Apply for NPI-verified access to our 503A formulary. Our team reviews each application within 1 to 3 business days.
Licensed healthcare providers only · NPI verification required · Miami-based. Exosome formulations and devices ship nationwide; compounded preparations ship only where our pharmacy partner holds a license
How this material is characterized
The release testing and handling standards behind compounded injectables, and what a supplier should be able to document on request.
- Sterility, Endotoxin, and Mycoplasma Testing
Three tests, three different questions, three blind spots.
- Cold Chain Validation and Storage
Storage, excursion tolerance, and receiving checks.
Peptides & Small Molecules FAQ
- How do medical practices order compounded formulations through ExaVeyra?
- ExaVeyra refers licensed prescribers to our 503A pharmacy partner. A licensed prescriber creates a portal account and verifies their NPI, and our team reviews the practice before releasing the formulary and pricing. Each preparation is then compounded by a licensed 503A pharmacy against a valid prescription for an individual patient. ExaVeyra does not hold or resell compounded preparations.
- What quality documentation comes with a compounded formulation?
- A certificate of analysis covering purity, potency and, for sterile preparations, sterility is available on request for every lot, together with the lot number. Our organic chemist reviews the documentation before a formulation is added to the formulary.
- Are compounded formulations sourced compliantly?
- Each preparation is compounded by a 503A pharmacy licensed by its state Board of Pharmacy, against a valid prescription for an individual patient, with documentation that supports your practice's recordkeeping. Practitioners prescribe within their own scope and regulatory obligations. Our team can walk your practice through how the service works before your first prescription.
- What formats are available?
- Depending on the compound, the pharmacy prepares injectable, capsule, tablet, troche, cream and solution formats. Strengths, fill volumes and beyond-use dates for each preparation are listed in the formulary released to verified practices.
- How are compounded preparations shipped and stored?
- The dispensing 503A pharmacy ships each prescription in temperature-controlled, lot-tracked packaging, with the storage conditions and beyond-use date on the label. ExaVeyra does not hold compounded preparations.
Regulatory notice
Compounded preparations. Compounded preparations are not FDA-approved, and the FDA does not verify their safety, effectiveness or quality before they are dispensed. Each preparation is compounded and dispensed by our 503A pharmacy partner, licensed by its state Board of Pharmacy, on a patient-specific prescription from a licensed prescriber; ExaVeyra Sciences does not compound, dispense or prescribe. ExaVeyra makes no claim that any preparation is safe or effective for any condition. Availability depends on the pharmacy’s license in the destination state and on whether the substance may be compounded under federal and state law. Prescribing, patient selection and scope of practice are the responsibility of the licensed prescriber. ExaVeyra Sciences is a supplier: it does not provide medical care, does not consult with patients and takes no part in clinical decisions.
Compounded hormone and GLP-1 preparations. Compounded hormone and GLP-1 preparations are not FDA-approved and are not interchangeable with FDA-approved products; where an approved product exists, any difference from it is the prescriber’s determination for an individual patient. Each preparation is compounded and dispensed by our 503A pharmacy partner on a patient-specific prescription. ExaVeyra makes no claim that any preparation is safe or effective for any condition. Availability depends on the pharmacy’s license in the destination state, on whether the substance may be compounded under federal and state law, and on current FDA policy for the agent prescribed. ExaVeyra Sciences is a supplier: it does not provide medical care, does not consult with patients and takes no part in clinical decisions.
All compounded formulations are prepared by a licensed 503A sterile compounding pharmacy partner. Compounds are available to NPI-verified licensed practitioners only. Formulations are compounded per individual patient prescriptions in accordance with applicable state and federal law. Compounded medications are not FDA-approved. Pricing available upon verified account approval.
Compounded preparations are not FDA-approved, and the FDA does not verify their safety, effectiveness or quality before they are dispensed. Each is compounded and dispensed by a licensed 503A pharmacy against a patient-specific prescription. This page is for informational purposes only and is not medical advice. For licensed healthcare providers only. NPI verification required for formulary access.




