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The Oral NAD+ Precursor

NMN

Also known as β-NMN · Nicotinamide mononucleotide

Summary coverage

At a glance

What it is
Oral NAD+ precursor with real biochemical data. Not the same as injectable NAD+.
Evidence
Small human studiesHow the tiers workA randomised trial in Nature Metabolism, January 2026 (NCT05517122, n=65, 14 days) found NMN at 1,000 mg/day and nicotinamide riboside at 1,000 mg/day each roughly doubled whole-blood NAD+, increases of about 43.1 and 49.4 micromoles per litre, while nicotinamide at 500 mg/day did not. Why this tier
Half-life
Not established in available literature
Routes
Oral
Category
Longevity
FDA
Not nominated
As of 3 August 2026. What that means
WADA
We do not state a status

Putting NMN on a schedule, with the vial it comes from and a log of each dose, happens in the app: Claritide for iPhone.

Evidence

Why this tier

A randomised trial in Nature Metabolism, January 2026 (NCT05517122, n=65, 14 days) found NMN at 1,000 mg/day and nicotinamide riboside at 1,000 mg/day each roughly doubled whole-blood NAD+, increases of about 43.1 and 49.4 micromoles per litre, while nicotinamide at 500 mg/day did not. The 2026 PRISMA review of 113 studies confirms consistent biochemical target engagement and good tolerability over weeks to months, alongside heterogeneous and often null effects on functional, metabolic and vascular outcomes. Recent trials cover retinal thickness in older people with diabetes, immune thrombocytopenia, a blood-pressure meta-analysis and blood-flow-restriction exercise inflammation.

Overview

What it is

NMN is an oral NAD+ precursor and it is constantly confused with injectable NAD+. The distinction matters because the evidence genuinely differs by route: oral NMN roughly doubles whole-blood NAD+ in a randomised trial, while no outcomes trial has evaluated intravenous or intramuscular NAD+ itself for wellness indications. The biochemistry works; what it translates into is less clear.

Mechanism

How it works

NMN is one step from NAD+ in the salvage pathway, and it is taken orally. The proposed route into the body is less direct than the name suggests: rather than being absorbed intact and converted, gut microbial conversion to nicotinic acid via the Preiss-Handler pathway is the leading explanation for how oral NMN raises circulating NAD+. Either way, the endpoint has been measured: whole-blood NAD+ rises, which is more than can be said for the injectable parent molecule.

Dosing

Commonly researched ranges

These are figures reported in published literature and practitioner protocols: a commonly researched range, not a recommendation. Claritide does not tell you what to take.
  • Randomised trial doses250–900 mg

    Once daily, 6 to 12 weeks in the published trials

    The published arms are 250 mg (Igarashi 2022), and 300, 600 and 900 mg (Yi 2023, GeroScience). The response plateaus around 600 mg/day, since 900 mg did not clearly beat it, which is the useful part of the finding. Stated first because the 1000 mg row below is a single 14-day study, not the band four randomised trials converge on.

  • Randomised trial dose · 1000 mg1000 mg

    Daily for 14 days

    The dose in NCT05517122, which roughly doubled whole-blood NAD+ (about +43.1 micromoles per litre). Nicotinamide riboside at the same dose did the same; nicotinamide at 500 mg/day did not.

Cycle guidance
Not established in available literature
Goals
Longevity, Energy
Legal standing

Where this sits with the FDA

Dated, sourced, and separate from whether it works. Removal from a warning list is not permission to compound.
Not nominatedas of 3 August 2026 · US

NMN is sold as an oral supplement rather than as an approved drug, and it does not appear on FDA’s compounding category lists. Its regulatory position as a dietary ingredient has been contested in the US; our sources do not resolve that, so we do not state it.

Primary source
Sport

WADA status

The 2026 Prohibited List entered force on 1 January 2026.
We do not state a status

Not named on the 2026 Prohibited List. We could not determine a classification and do not state one.

We looked and could not resolve it. This is not the same as "not prohibited". Treat it as unresolved and check with your federation before competing.

Reconstitution

There is nothing to mix

Not applicable. None of the published routes for this compound take a diluent, so there is no concentration to calculate and no beyond-use window to track.

Expectations

Week by week

What our material describes people reporting. Individual responses vary widely.

Not established in available literature.

Tolerability

Side effects

Grouped by how often our sources report them. Percentages appear only where a published trial figure exists.

Not established in available literature. Absence from this page does not mean absence of risk. It means our sources publish no side-effect profile for NMN.

Safety

Contraindications and interactions

Do not use if

Not established in available literature.

Interactions

Not established in available literature.

Absence from this list does NOT mean safety. It means lack of research.

Handling

Storage and cost

Storage
An oral supplement. There is no diluent, concentration or beyond-use window.
Cost
Not established in available literature
Combinations

Stacks with

Only pairings our own material actually documents. Stacking is the least evidence-based part of this field.
Deep dive

NMN in full

Limited coverage

NMN, beta-nicotinamide mononucleotide, is an oral NAD+ precursor. It ships as a separate record from injectable NAD+ for one reason: the evidence genuinely differs by route, and the two are constantly conflated.

What the trial showed

Nature Metabolism, January 2026. NCT05517122, 65 participants, 14 days. NMN at 1,000 mg/day and nicotinamide riboside at 1,000 mg/day each roughly doubled whole-blood NAD+, increases of about 43.1 and 49.4 micromoles per litre. Nicotinamide at 500 mg/day did not.

The proposed mechanism is not the obvious one. Rather than being absorbed intact, the leading explanation is gut microbial conversion to nicotinic acid via the Preiss-Handler pathway.

What that does not tell you

The 2026 PRISMA systematic review of 113 studies is the honest summary: consistent biochemical target engagement and good tolerability over weeks to months, alongside heterogeneous and often null effects on functional, metabolic and vascular outcomes.

In plain terms: it does the thing it says on the tin at the level of a blood test, and whether that makes you healthier is unresolved.

The contrast worth holding

Oral NMN: a randomised trial with a measured biochemical endpoint. Injectable NAD+: no eligible outcomes trials at all for anti-ageing or wellness indications, by FDA-independent systematic review.

The injectable is the one that costs several hundred dollars an infusion.

References

Sources

  1. 1
    Nature Metabolism, January 2026 · NCT05517122, n=65, oral NMN and NR each roughly doubled whole-blood NAD+
  2. 2
    Ageing Research Reviews, April 2026 · PRISMA review of 113 NAD+ studies
  3. 3
    Yi et al., 2023, GeroScience · 300, 600 and 900 mg/day for 60 days; walking distance and blood NAD+ rose, with the response levelling off near 600 mg (dose review, 2026-08-17)
  4. 4
    Igarashi et al., 2022, npj Aging · 250 mg/day in older men (dose review, 2026-08-17)
  5. 5
    Fukamizu et al., 2022, Scientific Reports · 1250 mg/day shown safe over four weeks, the top of the tested range (dose review, 2026-08-17)

Every record in this library is free to read, and it stays free. Your own schedule, vials and log live in the app: Claritide for iPhone.