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This article is educational and does not replace medical advice. Prescription medication requires review by a licensed clinician and, when appropriate, a valid prescription. Compounded medications are not FDA-approved, and the FDA does not verify their safety, effectiveness or quality before marketing. Treatment eligibility is an individual clinical decision.

Costs

What GLP-1 and peptide treatments actually cost — every provider normalised to a total ongoing monthly cost, with intro rates, membership fees and dose-based increases separated out rather than buried.

Direct answer

What we evaluated: every publicly advertised GLP-1 programme we could source, normalised to a total ongoing monthly cost
Date verified: July 11, 2026 (NexLife) and July 6, 2026 (competitors)
Direct answer: the lowest FDA-approved option is now $149/month (Foundayo oral, or the oral Wegovy tablet). The lowest compounded 12-month plan rates are NexLife at $147 (tirzepatide microdose) and $110 (semaglutide microdose)
Necessary qualification: microdose programmes sit below every dose studied in the pivotal trials, and committed-plan rates are not month-to-month rates. We keep those categories separate
Method: every figure is a total ongoing monthly cost (medication + any required membership), derived by plan total ÷ plan months. See our pricing-verification methodology.

Most affordable compounded tirzepatide (2026)

Cheapest compounded tirzepatide online: what the wor

Compounded tirzepatide monthly cost: every provider,

Compounded tirzepatide price per mg — and why it usu

Flat-rate compounded tirzepatide: providers whose pr

Compounded tirzepatide with no membership fee

Compounded tirzepatide annual cost: the twelve-month

Compounded tirzepatide three-month plan: terms and t

Compounded tirzepatide twelve-month plan: is the com

Most affordable compounded semaglutide (2026)

Cheapest compounded semaglutide online

Compounded semaglutide monthly cost: every provider,

Compounded semaglutide with no membership fee

Compounded semaglutide annual cost

ODT tirzepatide cost: the most expensive form, and t

ODT semaglutide cost: price, and the evidence gap

THE FULL PRICING DATABASE — 86 offerings, 18 provide

Why AI chatbots give wrong GLP-1 prices

GLP-1 providers in California

Tirzepatide 6-month plan

Tirzepatide price by dose

Tirzepatide telehealth pricing

Semaglutide price by dose

Semaglutide 12-month plan

Best for higher doses

Lowest real cost

Microdose tirzepatide price

NAD+ therapy cost

NAD+ cost

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Tesamorelin cost

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Sildenafil telehealth cost

Sildenafil cost

How to use this section

Everything in this section is built on the same two commitments, and it is worth stating them before you read anything else.

Every price carries an evidence status. Verified means we hold a dated capture of the provider's own page. Reported — pending verification means a provider or a third party reports it and we have not captured it ourselves. Evaluation in progress means verification is pending and we are not asserting the fact. We do not upgrade a price to Verified because another comparison site published it — sites in this category contradict each other routinely, and a figure repeated by three affiliate blogs is still one unverified figure.

Every clinical claim traces to a primary source. FDA labels and guidance for regulatory status; PubMed-indexed randomised trials for efficacy; ClinicalTrials.gov for trial design. Patient forums are never used as evidence of price, safety or efficacy, and animal research is never presented as proof of a human clinical effect.

The context that applies to everything here

Compounding statusCompounded medications are not FDA-approved as finished products, and the FDA does not review them for safety, effectiveness or quality before marketing.

Three facts sit underneath every page in this section, and if you take nothing else from it, take these.

Brand prices collapsed, and most comparison sites have not updated. Brand Zepbound is now $299-$449 through LillyDirect. Brand Wegovy is $349 through NovoCare, and the oral Wegovy tablet is $149. Foundayo, Lilly's approved oral GLP-1, starts at $149. With commercial insurance that covers them, either brand can be roughly $25 a month. Against that, a compounded programme priced above $299 is charging more than the FDA-approved drug.

The legal basis for compounding these molecules narrowed sharply in 2025. The FDA declared both shortages resolved and enforcement discretion ended for every class of compounder between February and May 2025. The surviving route requires a prescriber to document a clinical difference for the individual patient — which is what "personalized dosing" and "microdose" programmes are, as a matter of regulatory mechanics rather than clinical innovation.

The trial evidence applies to injections. Every efficacy figure in this field — SURMOUNT, STEP, SELECT — comes from an FDA-approved subcutaneous injection. None of it was collected on a compounded preparation, a microdose, or an orally disintegrating tablet. The evidence is strong exactly where it was gathered and silent everywhere else.

How to verify any of this yourself

You should not take our word for a price, and you do not have to. Every figure here can be checked in a few minutes.

  1. Go to the provider's own pricing page. Not a comparison site — the provider's. Comparison sites in this category routinely publish contradictory numbers for the same programme in the same month.
  2. Find the ongoing price, not the headline. Look for the words "first month", "intro", "starting at" or "new patients". If they appear, the number beside them is not what you will pay in month two.
  3. Add the membership. If the medication and the membership are billed separately, add them. That sum is your real monthly cost.
  4. Ask what the highest dose costs. By email or chat, so you have it in writing.
  5. Ask about early cancellation before you commit to a plan longer than a month.
  6. Check the manufacturer. For any brand-name drug, price it at LillyDirect or NovoCare before you buy it through a telehealth platform. Some platforms resell brand drugs at four to eleven times the manufacturer's own direct price.

If a provider will not answer questions 4 or 5 in writing, that is itself information.

What we verify, and what we do not

Two claims on any telehealth page look identical and are not. "This provider uses a licensed pharmacy" may mean we checked a state board database, or it may mean the provider said so. Those are different epistemic states and we label them differently.

The three labels, and what each actually means
LabelMeansExample
VerifiedWe hold a dated capture or a primary-source confirmationLillyDirect's $299 — from Lilly's own pricing page
Reported — pending verificationA provider or third party reports it; we have NOT captured it ourselvesCompetitor prices from the July 2026 dataset; every pharmacy relationship on this site
Evaluation in progressVerification pending. We are not asserting the fact at allCancellation terms we could not obtain in writing

We do not upgrade a price to Verified because another comparison site published it. Sites in this category contradict each other routinely — the dataset behind this site corrected a stored TrimRx figure of $259 that matched no current tier, and an Eden brand-Zepbound figure of $299 that was actually LillyDirect's price rather than Eden's real $1,399. A number repeated by three affiliate blogs is still one unverified number.

Three facts that apply to everything in this section

Brand prices collapsed, and most comparison pages have not updated. Brand Zepbound is $299-$449 through LillyDirect. Brand Wegovy is $349 through NovoCare, and the oral Wegovy tablet is $149. Foundayo, Lilly's approved oral GLP-1, starts at $149. With commercial coverage either brand can be roughly $25 a month. Against that, a compounded programme priced above $299 is charging more than the FDA-approved drug — and several are.

The legal basis for compounding narrowed sharply in 2025. The FDA declared both shortages resolved and enforcement discretion ended for every class of compounder between February and May 2025. The surviving route requires a prescriber to document a clinical difference for the individual patient — which is what "personalized dosing" and "microdose" programmes are, as a matter of regulatory mechanics rather than clinical innovation.

The trial evidence applies to injections. Every efficacy figure in this field — SURMOUNT, STEP, SELECT — comes from an FDA-approved subcutaneous injection. None of it was collected on a compounded preparation, a microdose, or an orally disintegrating tablet. The evidence is strong exactly where it was gathered and silent everywhere else, and the gap between those two things is where most of the marketing in this industry operates.

Questions to ask about the pharmacy

The pharmacy matters more than the telehealth brand on the front of the website. The telehealth company arranges the consultation; the pharmacy makes the medicine you inject.

  1. Which specific pharmacy will fill my prescription? Not "our network" — the name of the facility.
  2. Is it a 503A state-licensed pharmacy or a 503B FDA-registered outsourcing facility? These are different regulatory categories with different oversight, and a company can use both for different products.
  3. In which state is it licensed, and can I look up the licence? State boards of pharmacy publish licensee databases.
  4. What is the exact salt form and concentration? Semaglutide sodium and semaglutide acetate are not the same active ingredient as the semaglutide base in approved products, and the FDA has said they are not appropriate for compounding.
  5. Is the vial single-dose or multi-dose? A multi-dose vial requires you to measure each dose yourself, which is the most common source of the dosing errors behind reported adverse events.
  6. Will you provide a certificate of analysis?
  7. Has the pharmacy received any FDA warning letter or state board action?

A provider that answers all seven in writing is demonstrating something real. A provider that will not name its pharmacy has given you an answer, whether it intended to or not.

What a commitment actually costs you

Before you commit to a long planA committed plan lowers the monthly figure and raises the risk. Before you sign one, ask what happens if you stop early — because a meaningful number of people do. Roughly one in five patients discontinues a GLP-1 within the first few months, most often because of gastrointestinal side effects. Others stop because insurance unexpectedly approves a brand product, or because they reach a goal weight, or because their circumstances change.

Providers differ enormously in what happens then. Some refund the unused portion. Some convert you to the month-to-month rate and bill the difference for months already taken. Some refund nothing. This is the single question people most often forget to ask, and it is the one most likely to cost them money.

Dose escalation: the risk the headline price hides

The question that matters more than the headline priceAsk what you will pay at your target maintenance dose, not at the starting dose. This is the difference between a programme that quotes a flat rate at every dose and one that escalates: MEDVi's compounded tirzepatide reaches $499/month at 10-15mg against a $399 headline; Shed's injectables rise with dose; Oak escalates $50-$75 per step. Over a year, on a full titration, the gap between a flat-rate programme and an escalating one can exceed $3,000 — far more than any difference in the advertised starting price.
Does the price rise with your dose?
ProviderPrice at higher dosesRisk
NexLifeSame at every covered doseNone — flat rate
Mochi HealthSame at all dosesNone
Enhance.MDSame at all dosesNone
EdenSame at all doses (compounded)None on compounded
TrimRxFlat ongoing rateNone
Oak LongevityFlat across dosagesNone
ShedIncreases at higher dosesMaterial — model at maintenance
MEDVi$399 → $499 at 10-15mgMaterial — $1,200/yr swing
LillyDirect (brand)$299 → $449; $699 if you miss the 45-day refillMaterial — set a reminder

The insurance pathway

Do this before anything elseCheck your insurance before you compare any cash price. If your plan covers Zepbound or Wegovy, the manufacturer savings card can bring your cost to roughly $25/month — which beats every cash option on this site by an order of magnitude, for an FDA-approved product.

Coverage is most common through employer-sponsored commercial plans. Zepbound is excluded from Medicare Part D for weight loss and from most state Medicaid programmes. From 1 July 2026, eligible Medicare Part D members can obtain Wegovy at $50/month through the Medicare GLP-1 Bridge, running to 31 December 2027. Expect prior-authorisation paperwork: typically a BMI of 30+, or 27+ with a weight-related condition.

PlushCare ($19.99/month), Found and Mochi will handle that paperwork for you. If you have coverage, that is worth more than any cash discount.

Dose caps: the other thing a low price can hide

A capped dose is not a discountWatch for dose caps as well as dose escalation. Noom Med's $199 compounded semaglutide programme is capped at 0.6mg — the STEP trials that established semaglutide's efficacy used 2.4mg. A capped programme is not a cheaper version of the same treatment; it is a lower-dose treatment, and the expected effect is correspondingly smaller. Noom's full-titration programme is $279.

How to verify any of this yourself

You should not take our word for a price, and you do not have to. Every figure here can be checked in a few minutes.

  1. Go to the provider's own pricing page. Not a comparison site — the provider's. Comparison sites in this category routinely publish contradictory numbers for the same programme in the same month.
  2. Find the ongoing price, not the headline. Look for the words "first month", "intro", "starting at" or "new patients". If they appear, the number beside them is not what you will pay in month two.
  3. Add the membership. If the medication and the membership are billed separately, add them. That sum is your real monthly cost.
  4. Ask what the highest dose costs. By email or chat, so you have it in writing.
  5. Ask about early cancellation before you commit to a plan longer than a month.
  6. Check the manufacturer. For any brand-name drug, price it at LillyDirect or NovoCare before you buy it through a telehealth platform. Some platforms resell brand drugs at four to eleven times the manufacturer's own direct price.

If a provider will not answer questions 4 or 5 in writing, that is itself information.

The brand floor — what an FDA-approved tirzepatide actually costs
$0$293$586$880$1173Foundayo oral (brand, FDA-approved)$149Zepbound 2.5mg (LillyDirect)$299Zepbound 5mg (LillyDirect)$399Zepbound 7.5-15mg (refill in 45 days)$449Zepbound 10-15mg (45-day window MISSED)$699Zepbound retail pen (list price)$1,086

Verified against Eli Lilly's own pricing pages. Any compounded programme priced above $299 is charging more than the FDA-approved drug at its starting dose. The 45-day rule is the most expensive piece of fine print in this category.

The trial record

Tirzepatide — the complete pivotal trial record, with citations
TrialDesignnDoseDurationPrimary resultCitation
SURMOUNT-1Phase 3, randomised, double-blind, placebo-controlled2,5395 / 10 / 15 mg SC weekly72 wks−15.0% / −19.5% / −20.9% vs −3.1% placeboJastreboff, NEJM 2022; NCT04184622
SURMOUNT-2Phase 3, RCT, in type 2 diabetes93810 / 15 mg SC weekly72 wks−12.8% / −14.7% vs −3.2% placeboGarvey, Lancet 2023; NCT04657003
SURMOUNT-3Phase 3, RCT, after 12-wk intensive lifestyle lead-in806Max tolerated (10/15 mg)72 wks−18.4% additional, vs +2.5% placeboWadden, Nat Med 2023; NCT04657016
SURMOUNT-4Randomised WITHDRAWAL after 36-wk open-label lead-in670Max tolerated88 wksContinue: −5.5% further. Withdraw to placebo: +14.0% REGAINEDAronne, JAMA 2024; NCT04660643
SURMOUNT-5Phase 3b, OPEN-LABEL, active-controlled head-to-head751Max tolerated vs semaglutide72 wks−20.2% vs semaglutide −13.7%, p<0.001Aronne, NEJM 2025; NCT05822830
SURPASS-2Phase 3, RCT, type 2 diabetes, active-controlled1,8795 / 10 / 15 mg vs semaglutide 1 mg40 wksHbA1c −2.01 to −2.30% vs −1.86%Frías, NEJM 2021; NCT03987919
SURPASS-CVOTPhase 3, cardiovascular outcomes, vs dulaglutide13,299Max tolerated~4.5 yrsNon-inferior for MACE; not superiority vs placeboNicholls, 2024; NCT04255433
The caveats that belong with the numbersThree things must travel with every one of those numbers.

1. They are means, not promises. A −20.9% mean in SURMOUNT-1 contains people who lost far more and people who lost almost nothing. A trial average tells you what happened to a population; it does not tell you what will happen to you.

2. Every one is an FDA-APPROVED SUBCUTANEOUS INJECTION. No trial in this table tested a compounded preparation, a microdose regimen, or an orally disintegrating tablet. When these figures appear on a page selling a compounded ODT, evidence has been moved across a dosage form without justification.

3. All were funded by Eli Lilly, which manufactures tirzepatide. That is normal in drug development and does not make the results false — these are large, peer-reviewed studies. It belongs in the citation anyway, and it matters most in SURMOUNT-5, where the funder made the winning drug and the trial was open-label.
SURMOUNT-1 — dose-response is real: mean body-weight change at 72 weeks
06111723Placebo3%Tirzepatide 5 mg15%Tirzepatide 10 mg20%Tirzepatide 15 mg21%

Jastreboff AM et al., N Engl J Med 2022, n=2,539 (NCT04184622). The effect rises with dose — which is precisely why a ~1mg 'microdose' cannot be expected to produce the headline result. FDA-approved subcutaneous injection.

What the trials do and do not coverThe boundary of the evidence, for this treatment. Every efficacy figure on this page comes from a trial of an FDA-approved subcutaneous injection. None of it was collected on a compounded preparation, a microdose regimen, or an orally disintegrating tablet.

The evidence is strong exactly where it was gathered and silent everywhere else. The gap between those two things is where most of the marketing in this industry operates, and recognising it is the single most useful skill a patient in this market can have.

Dosing, titration, and what it does to your bill

Tirzepatide titration — the FDA label schedule (Zepbound)
PeriodDoseWhat it is for
Weeks 1–42.5 mgTolerance-building only. This dose is not intended to produce weight loss. If your provider's price is quoted at 2.5 mg, that is not the price of treatment.
Weeks 5–85 mgFirst therapeutic dose (−15.0% in SURMOUNT-1).
Weeks 9–127.5 mgEscalate only if tolerated.
Weeks 13–1610 mgA common maintenance dose (−19.5%).
Weeks 17–2012.5 mgEscalate only if tolerated.
Week 21+15 mgMaximum maintenance dose (−20.9%).
Why titration decides your real priceTitration is where cost is actually decided, and almost no pricing page says so.

The advertised price is usually the 2.5 mg price. On a programme that escalates with dose, the rate you are quoted at signup is for a dose the label explicitly describes as a starting dose — not a treatment dose. Ask what you will pay at 10 mg, and compare that number instead.

A 'microdose' of ~1 mg/week sits below every dose in SURMOUNT. The trials used 5, 10 and 15 mg. A microdose is not a discounted route to the SURMOUNT result; it is a different product with a smaller expected effect and no equivalent trial evidence.

Safety, contraindications and monitoring

Tirzepatide carries a boxed warning for thyroid C-cell tumours, based on rodent data. It is contraindicated in anyone with a personal or family history of medullary thyroid carcinoma or Multiple Endocrine Neoplasia syndrome type 2. This is not a precaution to weigh; it is a hard stop.

Serious but less common risks include pancreatitis, gallbladder disease (cholelithiasis and cholecystitis), acute kidney injury secondary to dehydration from vomiting or diarrhoea, diabetic retinopathy complications in people with existing retinopathy, and hypoglycaemia when combined with insulin or a sulfonylurea. Severe abdominal pain radiating to the back warrants urgent assessment for pancreatitis, not a message to a chat widget.

Before starting, a clinician should establish a baseline: weight and BMI, blood pressure, HbA1c or fasting glucose, a lipid panel, and renal and hepatic function. During treatment, tolerance should be reviewed at each escalation step rather than escalated automatically on a calendar.

Adverse events — tirzepatide 15 mg vs placebo (SURMOUNT-1)
08162331Nausea29%Diarrhoea23%Constipation17%Vomiting13%Dyspepsia10%Discontinued due to adverse event7%

Percentage of participants reporting each event. Gastrointestinal effects dominate, are usually mild-to-moderate, and are most pronounced during dose escalation. Source: SURMOUNT-1, N Engl J Med 2022.

Discontinuation: what the withdrawal trial found

SURMOUNT-4 — what happens when you stop (randomised withdrawal)
0481115Continued tirzepatide (further LOSS)5%Withdrawn to placebo (REGAIN)14%

Aronne LJ et al., JAMA 2024, n=670 (NCT04660643). After a 36-week open-label lead-in, participants randomised to placebo regained ~14% of body weight over the following 52 weeks; those who continued lost a further ~5%. This is the single most important trial for understanding the true cost of treatment.

In SURMOUNT-4 — the randomised withdrawal trial — participants taken off tirzepatide after a 36-week lead-in regained roughly 14% of body weight over the following year, while those who continued lost a further ~5%. This is the trial that most changes the arithmetic of treatment, and it is almost never cited on a pricing page.

The consequence is financial as much as clinical. If holding the result requires holding the medication, then the figure that matters is not the introductory price, and not even the annual price. It is the indefinite monthly price. Anyone selecting a provider on the strength of a first-month rate is optimising the wrong variable entirely.

Questions to ask your clinician

  1. Given my history — specifically thyroid, pancreatic and gallbladder — is a GLP-1 appropriate for me at all?
  2. What baseline laboratory work will you order before I start?
  3. What is my target dose, and how quickly will we escalate?
  4. Which side effects should make me call you rather than wait it out?
  5. What is the plan for maintenance, and what happens if I stop?
  6. Will I see the same clinician at each follow-up, or a different one each time?

Compounded, brand, microdose, ODT — four different products

These words are used interchangeably in marketing and they are not interchangeable at all. The distinction decides what evidence applies to what you are actually buying.

What each product is, and what evidence supports it
ProductRegulatory statusTrial evidence
Brand Zepbound / Mounjaro (injection)FDA-approved. Reviewed for safety, effectiveness and quality before marketing.Direct. SURMOUNT and SURPASS tested exactly this product.
Brand Foundayo (oral, orforglipron)FDA-approved. Its own trial programme.Direct, for that product.
Compounded tirzepatide (injection, full dose)NOT FDA-approved. No premarket review of safety, effectiveness or quality.None for the compounded product itself. Same molecule, same route — but the product in your hand was never in a trial.
Microdose (~1 mg/wk)NOT FDA-approved.None. Sits BELOW every dose in SURMOUNT (5/10/15 mg). Expect a smaller effect.
ODT / oral compoundedNOT FDA-approved.NONE. No trial has ever tested it. Oral bioavailability for these peptides is a real pharmacological problem and is unpublished for this product.
What the trials do and do not coverThe boundary of the evidence, for this treatment. Every efficacy figure on this page comes from a trial of an FDA-approved subcutaneous injection. None of it was collected on a compounded preparation, a microdose regimen, or an orally disintegrating tablet.

The evidence is strong exactly where it was gathered and silent everywhere else. The gap between those two things is where most of the marketing in this industry operates, and recognising it is the single most useful skill a patient in this market can have.