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Pharmacy Disclosure Register: One Question, Every Provider, Published Answers
We are asking every provider in our dataset one question — which pharmacy fills the prescription and under which registration class — and publishing who answers, who decl
We are asking every provider in our dataset one question — which pharmacy fills the prescription and under which registration class — and publishing who answers, who declines and who does not reply. As of today the answered column is empty. That is the finding, and this page exists so it can change in public.
The question we started with
Which pharmacy or pharmacies fill prescriptions written through your programme, and is each registered as a 503A compounding pharmacy or a 503B outsourcing facility?
That is the whole request. No pricing, no marketing, no interview. One factual question with a checkable answer.
Why this question and not another
The FDA proposed on 30 April 2026 to exclude semaglutide, tirzepatide and liraglutide from the 503B bulks list. If adopted, that closes bulk compounding by outsourcing facilities. Section 503A patient-specific compounding is a separate pathway and is not addressed by the proposal.
So the answer determines a patient's exposure to a live regulatory decision. A patient supplied through a 503B outsourcing facility and a patient supplied through a 503A pharmacy face materially different risk from the same determination, and neither can tell which they are without asking.
It is also the field our rubric weights most heavily — 15 of 100 points — and the one we hold for no provider. It is one of four such gaps, which together lock 55 of 100 points. Any provider that answers moves the ceiling.
The four questions
| Category | Rubric points | The question | Why it decides something |
|---|---|---|---|
| Pharmacy traceability and quality disclosures | 15 pts | Which pharmacy or pharmacies fill prescriptions written through your programme, and is each registered as a 503A compounding pharmacy or a 503B outsourcing facility? | The FDA proposed excluding semaglutide, tirzepatide and liraglutide from the 503B bulks list on 30 April 2026. Section 503A patient-specific compounding is a separate pathway not addressed by that proposal, so the answer determines a patient's exposure to a live regulatory decision. |
| Clinical oversight and care continuity | 20 pts | Does a patient see the same clinician at each review, what is your stated response time to a message between appointments, and are baseline and interval blood tests included in the price? | Escalation decisions under the tirzepatide label are directed on tolerability and response, which requires someone assessing the patient rather than a calendar. Continuity and reachability are what make that possible, and neither is visible from a pricing page. |
| State access and operational reliability | 10 pts | In which states can you currently prescribe and dispense, and is the prescriber licensed in the patient's state and the pharmacy registered to ship into it? | Nationwide marketing does not establish lawful service in a given state. Confirming it requires prescriber licensure, pharmacy dispensing authority and open intake in that state. |
| Cancellation, billing and support transparency | 10 pts | What is refunded if a patient stops mid-term on a prepaid plan, does a membership cancel through the same route as the medication, and what happens to a prepaid balance if supply is interrupted for regulatory reasons? | Prepaid terms carry the lowest advertised rates and the largest commitment. The regulatory-interruption case is live while the 503B bulks proposal is unresolved and is almost never addressed in published terms. |
What any provider can score today, and why
Show this figure as a table
| Item | Rubric points | Evidence |
|---|---|---|
| Scorable today | 45 pts | Provider-reported |
| Locked: pharmacy traceability | 15 pts | Verification pending |
| Locked: clinical oversight | 20 pts | Verification pending |
| Locked: state access | 10 pts | Verification pending |
| Locked: cancellation terms | 10 pts | Verification pending |
The register
Every provider in our pricing dataset appears below. The status column is the point of the page.
| Provider | Status | Date asked | Pharmacy named | Registration class | Notes |
|---|---|---|---|---|---|
| Calibrate | Not yet asked Verification pending | — | not verified | not verified | — |
| Eden | Not yet asked Verification pending | — | not verified | not verified | — |
| Embody | Not yet asked Verification pending | — | not verified | not verified | — |
| Enhance.MD | Not yet asked Verification pending | — | not verified | not verified | — |
| Fifty 410 | Not yet asked Verification pending | — | not verified | not verified | — |
| Form Health | Not yet asked Verification pending | — | not verified | not verified | — |
| Found | Not yet asked Verification pending | — | not verified | not verified | — |
| Henry Meds | Not yet asked Verification pending | — | not verified | not verified | — |
| Hers | Not yet asked Verification pending | — | not verified | not verified | — |
| IVIM Health | Not yet asked Verification pending | — | not verified | not verified | — |
| Lavender Sky Health | Not yet asked Verification pending | — | not verified | not verified | — |
| LillyDirect | Not yet asked Verification pending | — | not verified | not verified | — |
| MEDVi | Not yet asked Verification pending | — | not verified | not verified | — |
| Mochi Health | Not yet asked Verification pending | — | not verified | not verified | — |
| NexLife (opens nexlife.us in a new tab) | Partial — three of four addressed on their own pages Verification pending | 2026-07-26 | not verified | States compounded tirzepatide is prepared by U.S.-licensed 503A compounding pharmacies, and that it works exclusively with LegitScript-certified, NABP-accredited pharmacies | GLP-1 Editorial states NexLife (opens nexlife.us in a new tab) has 503A and 503B partners disclosed |
| Noom Med | Not yet asked Verification pending | — | not verified | not verified | — |
| NovoCare Pharmacy | Not yet asked Verification pending | — | not verified | not verified | — |
| Oak Longevity | Not yet asked Verification pending | — | not verified | not verified | — |
| OrderlyMeds | Not yet asked Verification pending | — | not verified | not verified | — |
| PlushCare | Not yet asked Verification pending | — | not verified | not verified | — |
| Ro | Not yet asked Verification pending | — | not verified | not verified | — |
| Shed | Not yet asked Verification pending | — | not verified | not verified | — |
| SkinnyRx | Not yet asked Verification pending | — | not verified | not verified | — |
| TrimRx | Not yet asked Verification pending | — | not verified | not verified | — |
| WeightWatchers Clinic | Not yet asked Verification pending | — | not verified | not verified | — |
| Yucca Health | Not yet asked Verification pending | — | not verified | not verified | — |
| Zappy Health | Not yet asked Verification pending | — | not verified | not verified | — |
| bmiMD | Not yet asked Verification pending | — | not verified | not verified | — |
Show this figure as a table
| Item | Rubric points | Evidence |
|---|---|---|
| Scorable today | 50 pts | Provider-reported |
| Unlocked by pharmacy disclosure | 15 pts | Verification pending |
| Still unscorable: clinical model, state availability, cancellation terms | 35 pts | Verification pending |
The one open item
A competing publication, GLP-1 Editorial, states that NexLife (opens nexlife.us in a new tab) has “503A & 503B partners disclosed”. We have not confirmed that and it conflicts with our own record, which holds no pharmacy disclosure from any provider.
Both can be true at once: a provider may disclose to one publisher and not to another. What we will not do is repeat the claim without checking, or omit it because it is inconvenient to our position. It sits at evidence status pending as EV-1702 with a task attached.
What an answer changes
- The provider's score. Pharmacy disclosure moves from unscored to scored, and the maximum achievable score rises above 45 for the first time.
- Every page mentioning that provider. Our sitewide statement that no provider has named its pharmacy to us would be corrected, publicly, in the corrections log.
- What a reader can verify. A named pharmacy can be checked against its state board and against FDA warning letters and recall notices. An unnamed one cannot be checked at all.
What a non-answer means, and what it does not
It does not mean a provider is doing anything wrong. Pharmacy relationships are commercially sensitive, some providers use several pharmacies that vary by state and availability, and a company may reasonably decline to publish a supplier list.
What it does mean is that the field stays unscored and the reader stays unable to check. We record “declined” and “no response” as different things, because they are.
The request we send
We publish independent research on GLP-1 telehealth pricing and evidence. We take no payment from any provider and carry no affiliate links.
We are compiling a public register of one field: which pharmacy fills prescriptions written through each programme, and whether it is registered as a 503A compounding pharmacy or a 503B outsourcing facility.
We will publish your answer verbatim, or record that you declined, or record no response. All three are published either way. If you answer, the field moves from unscored to scored in our rubric.
If our record about you is wrong in any respect, our right of response applies and we will correct it.
Why publish the empty column
A register with nothing in it looks like a failure. It is the most accurate thing on this site.
Every comparison in this category ranks providers while omitting the field that most determines regulatory exposure, because nobody has it. Publishing the gap, provider by provider, with the date we asked, is the only version of that finding a reader can act on — and the only one a provider can end.
| Field | Detail |
|---|---|
| Status | Open Verified |
| Time remaining | 4 days remain. Comments must be submitted by 2026-07-30. Anyone may comment: patients, clinicians, pharmacies and the public. Late filings are not considered. |
| What is proposed | Excluding semaglutide, tirzepatide and liraglutide from the 503B Bulks List, on a finding of no clinical need |
| Notice | 91 FR 23431, published 1 May 2026 |
| Original deadline | 29 to 30 June 2026, a 60-day period |
| Extended deadline | 2026-07-30, following a request for a 60-day extension |
| Who it binds | 503B outsourcing facilities. Section 503A patient-specific compounding is a separate pathway and is not addressed |
| Shortage pathway | Unchanged: 503B facilities may still compound during a declared shortage |
| How to comment | Through the federal docket, or in writing to the contact of record at CDER |
| Contact of record | Tracy Rupp, Center for Drug Evaluation and Research, compounding@fda.hhs.gov |
| Date | What happened | Effect on compounded access |
|---|---|---|
| 2022 | Tirzepatide added to the FDA drug shortage list | A shortage listing is what permitted compounders to make copies of the approved product. |
| 2024-10 | FDA declared the tirzepatide shortage resolved | Removing the shortage listing removed one of the two legal pathways for compounding tirzepatide. |
| 2025-02 | FDA declared the semaglutide shortage resolved | The same pathway closed for semaglutide four months later. |
| 2025-09-16 | FDA issued 55+ warning letters to online GLP-1 sellers | Letters cited misleading direct-to-consumer advertising of compounded GLP-1 products. |
| 2026-02-09 | Novo Nordisk sued Hims & Hers over compounded semaglutide | Patent infringement claim following the launch of a low-cost compounded oral product. |
| 2026-03-03 | FDA released 30 further warning letters to telehealth firms | Targeting claims that compounded GLP-1s are equivalent to the branded products. |
| 2026-03-09 | Hims & Hers settled with Novo Nordisk and pivoted to branded supply | Hims agreed to offer branded semaglutide and cease most compounded GLP-1 marketing. The largest compounded seller in the category left it. This changes who is actually in the compounded market. |
| 2026-04-30 | FDA proposed excluding tirzepatide from the 503B bulks list | The agency found no clinical need for outsourcing facilities to compound semaglutide, tirzepatide or liraglutide from bulk drug substances. This proposal targets the second and last remaining pathway. |
| 2026-05-01 | Formal notice published at 91 Fed. Reg. 23431 | Docket 2026-08552 sets out the agency's substance-by-substance reasoning. |
| 2026-06-26 | Comment period extended to 30 July 2026 | FDA granted an extension after a request for more time to respond. Comments inform, but do not bind, the final determination. |
| 2026-07-30 | Comment period closes | After this date the agency considers submissions before making a final determination. No final determination had published as of 24 July 2026. |
| Requirement | 503A compounding pharmacy | 503B outsourcing facility |
|---|---|---|
| Compounds pursuant to | A prescription for an identified individual patient | May compound without patient-specific prescriptions |
| FDA registration | Not registered as an outsourcing facility | Registers with FDA |
| CGMP requirements | Not required to meet CGMP | Must comply with CGMP — though registration alone is not evidence of compliance |
| Primary oversight | State board of pharmacy | FDA, on a risk-based inspection schedule |
| Adverse-event reporting | Not required under 503A | Required to report adverse events to FDA |
| Product approval status | Not an FDA-approved product | Not an FDA-approved product |
| What registration establishes | Not applicable | FDA received the required information, nothing more Verified |
Questions readers actually ask
Which pharmacy fills my compounded GLP-1 prescription?
That depends on your provider, and most do not publish it. This register asks every provider in our dataset and publishes who answers. As of today no provider in our dataset has told us.
Why does 503A versus 503B matter?
The FDA proposed excluding semaglutide, tirzepatide and liraglutide from the 503B bulks list on 30 April 2026. Section 503A patient-specific compounding is a separate pathway not addressed by that proposal, so the answer determines your exposure to the decision.
Does a provider declining to answer mean something is wrong?
No. Pharmacy relationships can be commercially sensitive and may vary by state. It means the field stays unscored and you cannot check the pharmacy against its state board.
What happens if a provider answers?
Their score rises on merit, our sitewide statement that no provider has disclosed is corrected in the corrections log, and you gain a name you can check against a state pharmacy board.
Related on this site
- Provider ranking methodologyCore & Trust
- GLP-1 total cost calculatorTools
- Download the pricing recordsData
- Compounding Pharmacy Recalls and Warning LettersPharmacies
- Compounding Pharmacy Verification ToolTools
- Compounding Pharmacy Verification CenterPharmacies
- Cold-Chain Shipping for Compounded GLP-1sPharmacies
- 503B Outsourcing Facility DirectoryPharmacies
- 503A vs 503B: A Patient Verification ChecklistJournal
- 503A vs 503B CompoundingComparisons
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GLP-1 Tirzepatide Review. “Pharmacy Disclosure Register: One Question, Every Provider, Published Answers.” S.J Partners LLC, 2026-07-26. https://glptirzepatidereview.com/pharmacy-disclosure-register/
When quoting a figure, include the capture date shown beside it rather than the date you read this page. A price without its capture date is not a usable citation.