Information only — no products are sold on this website.
Cellular metabolism research
A coenzyme central to cellular energy metabolism. Widely studied in ageing biology; injectable and infusion presentations are not established approved therapies.
Nicotinamide adenine dinucleotide (NAD+) is a coenzyme present in all living cells and central to redox metabolism. Oral precursors are sold as supplements in many markets; injectable and IV presentations sit in a different regulatory category.
NAD+ participates in redox reactions and serves as a substrate for sirtuins and PARP enzymes, pathways studied in ageing and metabolic research.
Human research largely concerns oral precursors and reports biomarker changes; clinical-outcome evidence remains emerging. Evidence for injectable or IV NAD+ delivering claimed benefits is limited.
Infusion-related reactions are described anecdotally. Parenteral administration should only occur in an appropriate clinical setting. Safety information for this compound is incomplete outside of controlled settings. Reported considerations in the literature include injection-site reactions, unknown long-term effects, product-quality and sterility risks with unregistered preparations, and unpredictable interactions with existing medicines or conditions. Any consideration of use belongs with a registered healthcare professional who can assess the individual clinical picture.
Regulatory classification differs between oral supplement forms and injectable presentations, and between countries. Confirm locally.
Third-party analytical documentation for this compound is published for transparency and professional review. It confirms identity and purity of tested material only, and is not a marketing authorisation, a registration, or a recommendation for use.
View certificate (PDF)Evidence & Regulation
Every source below is a public, primary source — a literature index, a trials registry, or a regulator. They are reading directions for professionals, not endorsements, and they do not establish that any use of NAD+ is approved, safe or appropriate.
LiteratureIndependent index of published studies. Most entries for research peptides are preclinical.
RegulatorExplains registration, and the Section 21 route by which a healthcare professional may apply to access an unregistered product for a named patient.
RegulatorSeveral peptides have been placed in FDA categories that restrict compounding due to safety or characterisation concerns.
In South Africa, a product intended to treat, prevent or otherwise affect the functioning of the body is a medicine and must be registered with SAHPRA before it may lawfully be sold. An unregistered compound cannot be advertised or supplied to the public, regardless of the evidence behind it.
SAHPRA — medicines registrationWhere no registered alternative exists, a registered healthcare professional may apply to SAHPRA under Section 21 for authorisation to access an unregistered product for a named patient. That application is made by the clinician, not by the patient, and not by us.
Section 21 pathwayAny prescribing decision, dosing decision and dispensing step belongs to a registered healthcare professional and a licensed pharmacy. We publish reference information and analytical documentation only, and never dosing, protocols or self-administration guidance.
Non-approved substances are prohibited at all times under the World Anti-Doping Code, including many research peptides. Athletes under testing jurisdiction should treat every compound on this site as prohibited unless their governing body confirms otherwise.
WADA Prohibited ListA compound may be an approved medicine in one country, an investigational agent in a second, and an unregistered research chemical in a third. Always confirm the classification that applies where you practise before acting on any information here.
EMA medicines databaseInformation only — availability subject to applicable law, prescription/authorisation, and licensed healthcare/pharmacy channels. Nothing on this page is an offer to sell, and no dosing or self-administration guidance is provided.
South Africa — compliance notice
SAHPRA has publicly warned about unregistered peptide products being marketed to the South African public. In general, products intended to diagnose, treat, or otherwise alter bodily functions require registration or authorisation before they may lawfully be sold. ELLIVON BIOSCIENCES publishes reference information only and directs all clinical questions to registered healthcare professionals and licensed pharmacy channels.