Tirzepatide, checked
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Checklist for any clinic

Tirzepatide specialists: question cards for checking care

Use these cards with any clinic you are considering, in person or through telehealth, meaning care over video, phone or an online form. Each card covers one part: the prescriber who writes the prescription, the pharmacy, the medicine, the health check, what to watch for and the price. This guide does not rank, list or connect readers with clinics.

Start the checks
Pastel question cards arranged on a white desk with soft painted clouds
One check at a time: person, pharmacy, product, plan and price.

Six short checks

Check a service in clear passes

Going in order is easiest, but each card stands on its own, so start with the one you need most. Write down the answer, then verify the parts that have a public record. A polished website is not a record.

Pass A · Prescriber

Name the person responsible for the care

  • Who will assess me, and what are their full name and licence type?
  • Which state issued the licence?
  • Will that licence cover the state where I am during the visit?

Every state has a medical board that publishes physician licence status and public discipline.

A clean public record means no public action is shown; it is not a rating of the clinician’s care.

Find the medical-board route
Name and licence

Pass B · Pharmacy

Make the pharmacy visible

  • Which pharmacy makes and sends the medicine?
  • Is it an ordinary pharmacy that makes medicine for one patient at a time, or a larger facility that makes batches?
  • Can I verify its licence in my state?

As of September 2026, an ordinary pharmacy that made medicine to order for one named patient with a prescription was often called a 503A pharmacy. The name comes from the section of the law that allows it.

As of September 2026, a larger facility called a 503B outsourcing facility could make batches without a prescription for each patient. It had to follow the quality rules that drug factories follow, and FDA inspected it. Knowing which kind you are dealing with tells you which record to check: a state pharmacy licence, or FDA’s list of registered facilities.

As of September 2026, being registered with FDA did not mean FDA had approved the facility or its medicines. A state pharmacy licence was a separate check.

Use FDA’s state pharmacy links Check FDA’s list of batch facilities
Pharmacy and state

Pass C · Product

Get the exact name, form and maker

  • Is this Mounjaro, Zepbound or a compounded (pharmacy-made) preparation?
  • Who made it, and which form will be dispensed?
  • Why is this product being proposed for my reason for treatment?

As of September 2026, FDA-approved tirzepatide came under the Mounjaro and Zepbound names in pens and vials.

As of September 2026, anything not made by Lilly was not an FDA-approved tirzepatide product.

As of September 2026, compounded medicine could serve an individual need, but it was not FDA-approved.

As of September 2026, “FDA registered” did not mean “FDA approved.”
Product, form and maker

Pass D · Assessment

Test whether this is care or checkout

  • Can I ask the clinician my own follow-up questions?
  • How will the clinician decide whether tests or an exam are needed?
  • What happens if remote care is not enough?

In May 2026, the national group of state medical boards issued guidance on prescribing. It said picking a treatment from a list of options, with no real health check, is not proper care.

The same guidance says patients need a way to ask follow-up questions.

A tick-box form on its own is a warning sign. If the clinician never asks you follow-up questions about your health, it is not a proper assessment.

Pass E · Safety

Make the safety plan specific

  • Which parts of my history change this choice?
  • Which problems mean I need to call, and where do I call?
  • How will follow-up work if side effects do not settle?
  • What needs to happen before a planned procedure or pregnancy?

The tirzepatide labels flag thyroid-cancer history, serious stomach trouble, pancreas and gallbladder trouble, diabetic eye disease, pregnancy, birth control pills, other diabetes medicines and upcoming surgery as topics for the prescriber.

Both labels also carry a boxed warning over thyroid tumors that turned up in rats, with the effect in humans unknown.

Read the Zepbound label
Follow-up contact and plan

Pass F · Cost

Ask for a total you can compare

  • What is the full first-month cost?
  • What is the normal later-month cost?
  • Are the visit, medicine, labs, supplies, shipping and follow-up separate?
  • Does the quoted price expire or depend on refill timing?

As of September 26, 2026, Lilly’s cash prices for Zepbound, paid without insurance, ran from $299 to $699 a month. That covered vials or the KwikPen, a pen that holds four weekly doses. The price depended on the strength and on whether each refill was bought on time.

The same date, Lilly’s published list-price range was $499 to $1,086.37 per fill.

The list price is the maker’s official published price, and few people pay it. The cash price is what you would pay Lilly directly without insurance. With insurance, your share can be different again. These offers were due to expire on December 31, 2026.

First month
Later month

Warning cards

Know when to pause

One clear red flag is enough to ask more questions. Several together are a strong reason to leave.

A

No prescription

As of September 2026, selling a prescription medicine without a prescription was against federal law.

B

“Research use only”

As of September 2026, FDA had warned sellers that a research label did not turn a product marketed for human injection into a lawful medicine.

C

Approval word games

As of September 2026, a claim that a compounded drug was FDA-approved was false.

D

A hidden or false pharmacy

FDA has found fake compounded tirzepatide carrying labels that listed pharmacies which either did not exist or never made the product.

E

A form with no conversation

A form with no conversation is not enough. The clinician must be able to ask you follow-up questions and collect the health history that proper care needs.

Verification desk

Use the records that can answer the question

A licence lookup answers whether a licence exists. It does not measure quality of care. As of September 2026, an FDA registration answered whether a facility registered. It did not approve the facility or its drugs.

Prescriber

State medical board

Check the name, licence status and any public discipline in the official state record.

Find the board

Pharmacy

State pharmacy board

Use the FDA route to the state database and search the pharmacy name printed on the label.

Find the pharmacy record

Keep the context

Review the plain-language overview

Return to the short guide for approved uses, trial context, safety warnings and the price layers.

Back to start

Evidence drawer

Records for the checks

Assessment standard

The national group of state medical boards says a fixed online form, where every patient answers the same set questions, is not enough on its own. A clinician must be able to ask follow-up questions and get more history.

Open the telemedicine policy

Current guidance

Its May 2026 guidance adds that patients need the ability to ask a clinician follow-up questions.

Open the prescribing guidance

Registration

As of September 2026, a federal rule said that being registered with FDA did not mean FDA had approved the facility or its drugs. It also did not mean a product could be legally sold. To check a pharmacy, look up its state licence too.

Open the federal rule

Unapproved products

GLP-1 drugs are medicines, such as tirzepatide and semaglutide, that copy a natural gut hormone. FDA’s consumer page explains its concerns about pharmacy-made, fake and “research use only” versions of them.

Open the FDA concerns page