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NAD+ supplied as lyophilised powder in a multi-dose vial with matching injector pen, unbranded for private label

Longevity

NAD+

CoA per batch HPLC >=98% Private label available Laboratory and research use

NAD+ is supplied by White Label Peptides as a lyophilised powder in multi-dose vials, for laboratory and research use, to business buyers only. It sits in our longevity category. Every batch is verified by HPLC and ships with its own Certificate of Analysis.

CompoundNAD+
Full nameNicotinamide Adenine Dinucleotide
ClassificationCellular Energy and Metabolic Compound
Molecular formulaC21H27N7O14P2
Molecular weightApproximately 663.4 g/mol
StructureNAD+ is a naturally occurring coenzyme present in all living cells and plays a critical role in cellular energy production and metabolic function.
FormLyophilised powder (vials) or ready-to-use solution (pre-filled pens)
AppearanceWhite to off-white lyophilised powder prior to reconstitution
PresentationVials: 500 mg. Pre-filled pens: 500 mg, 1000 mg
ReconstitutionTypically reconstituted using: Bacteriostatic water - Sterile laboratory-grade water
StorageStore refrigerated at 2-8°C in a cool, dry environment away from direct sunlight. Long-term storage may require freezing conditions prior to reconstitution.
Compound TypeCoenzyme

Specification data is provided for identification and procurement. It is not dosing guidance and it is not a claim of any effect.

Evidence and status

Approval statusNot approved. It does not appear on the 503B bulks list, so drug products compounded with it are not eligible for the 503B exemptions. FDA has stated it is aware of compounders using food-grade NAD+ sold by repackagers to make intravenous products, and that food-grade ingredients are not suitable for sterile compounding
European statusNo European authorisation identified in this review
Strongest supportHuman tolerability data
Route contextIntravenous infusion in the published work, and subcutaneous in reported practice. The FDA's stated concern attaches to the intravenous route
Competitive sportNot established here. It is an endogenous coenzyme also sold as a food supplement, which complicates any classification. Verify with the relevant anti-doping organisation
  1. Lab work
  2. Animal studies
  3. Human studies
  4. Approved label

Reviewed 2026-09-02. Regulatory status is stated for procurement and varies by market. It is not legal advice.

Research

What the published literature examined

The published human work is about tolerability rather than effect. A retrospective pilot compared intravenous NAD+ against nicotinamide riboside in a real-world setting and recorded clinician- and participant-reported adverse experiences including nausea, diarrhoea, muscle cramping, chest pain and dizziness. A randomised placebo-controlled pilot examined acute intravenous administration in healthy adults. Related work has examined raising the NAD+ metabolome by oral precursors in a randomised triple-blind crossover design, which is a different question from administering the coenzyme itself.

What is not established

Systematic safety and tolerability investigation, which the published work says plainly remains limited despite widespread use. There is no standardised dose, no labelled route and no approved product. The oral-precursor literature does not transfer: raising the metabolome with a precursor and infusing the coenzyme are not the same intervention, and the studies that exist do not establish that they produce the same thing.

What distinguishes NAD+

This is the compound where the regulator's published concern is about the GRADE of the material rather than the molecule. FDA has said it is aware of food-grade NAD+ from repackagers being used to make injectables, and that food-grade material is not suitable for sterile work because of microbial and endotoxin contamination risk. For a buyer that reframes the question entirely: with this compound, what the certificate says about grade, endotoxin and bioburden is the product, and the molecule is the easy part.

Sources

  1. US FDA. FDA reminds compounders to use ingredients suitable for sterile compounding
  2. US FDA. Bulk drug substances used in compounding
  3. US FDA. Certain bulk drug substances for use in compounding that may present significant safety risks
  4. Intravenous infusion of nicotinamide adenine dinucleotide versus nicotinamide riboside: a retrospective tolerability pilot study in a real-world setting
  5. A combination of nicotinamide and D-ribose is safe and effective to increase the NAD+ metabolome in healthy middle-aged adults: randomised, triple-blind, placebo-controlled crossover pilot

This page describes a compound as a material and summarises published research about it. It is for general and procurement information only. It is not medical advice, not a treatment recommendation, and not guidance on use. Supplied for laboratory and research use, not for human consumption.

Specification

About this compound

The specification below is the batch-independent data. Purity and analysis date vary by batch, so they appear on the certificate issued with your order rather than on this page.

What this compound is

NAD+ in supply terms

NAD+, short for Nicotinamide Adenine Dinucleotide, is a dinucleotide compound built from a nicotinamide ring joined to an adenine ring through two linked ribose-phosphate units. The molecular formula C21H27N7O14P2 and a molecular weight of approximately 663.4 g/mol reflect this two-nucleotide backbone, and the compound is classed chemically as a coenzyme, a category defined by its dinucleotide structure rather than by any use claim. It occurs naturally across biological systems, and the material supplied here is manufactured to match that naturally occurring structure rather than being a synthetic analogue or fragment. It ships as a lyophilised powder in multi-dose vials at 500mg or 1000mg fill weights, well above the milligram fills typical of the shorter peptides on this list, reflecting its lower per-milligram cost of synthesis. Reconstitution uses bacteriostatic water or sterile laboratory-grade water. Store at 2-8C, away from direct sunlight, with freezing recommended for longer-term storage ahead of reconstitution. Buyers should compare quotes on a cost-per-gram basis given the larger fill weights, and confirm that the Certificate of Analysis specifies purity by HPLC rather than by mass alone.

This section describes the compound as a material. It makes no claim about any effect and is not guidance on use.

What varies by batch

The page identifies the compound. The certificate records the batch.

Purity, method, analysis date and issuing party belong on the batch record rather than in page copy.

Send the volume you need for NAD+ and your delivery country. We will quote against it.Request pricing

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Questions

Supply, answered

Is NAD+ available for private label?

Yes. It can be supplied under your own brand on the vial and the carton, with the Certificate of Analysis issued under your product name.

What is the minimum order quantity?

Set for this compound specifically and confirmed at the enquiry stage, before you commit.

What purity is supplied?

98 percent or higher, verified by HPLC. The certificate issued with your batch carries the actual figure for that batch.

How is it shipped?

As lyophilised powder in multi-dose vials, packed for transit. Delivery in 5 to 7 days once the batch is released.

We already buy NAD+. Can you quote against our current volume?

Yes. Send the volume and the delivery country. Pricing is tiered per compound, so the quote reflects what you buy rather than a list price.

Can you supply NAD+ as a second source?

Yes. Terms are agreed per compound, so you can add NAD+ without moving anything else you buy elsewhere.

Request pricing for NAD+

Indicative volume and delivery country is enough to start. We reply within one working day.

Anything else you already know. All optional.

We supply businesses across Europe, and we reply within one working day.