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Tafamidis Meglumine Capsule shortage

Tafamidis Meglumine Capsule is currently listed in shortage by the FDA. The FDA lists 1 affected product. This page was last refreshed from FDA data on Sep 18, 2026.

To Be Discontinued ⚠ Supply risk: High Cardiovascular 1 product 354 days First posted Sep 29, 2025 Updated Sep 29, 2025
Here’s the bottom line

Pfizer is stopping production of Vyndaquel (tafamidis meglumine) 20 mg capsules, with sales ending in December 2025. No other manufacturers of this product are listed, so there is currently no reported available source.

Don’t stop or change your therapy on your own — talk with your prescriber about the plan that fits you, and ask your pharmacist what’s actually available.

Do you take this drug? See the ‘What to do’ recommendation from Dr. Brian Staiger, PharmD →
1
Affected NDCs
1
Reporting manufacturers
0/1
Reporting mfrs supplying
0/1
Affected strengths supplied
354
Days in shortage
753
Medicaid Rx (2025)
Source: FDA Drug Shortages Database API (openFDA). Last refreshed Sep 18, 2026 · yesterday

What’s in shortage — at a glance

These figures count only the manufacturers that reported this shortage to the FDA — not every company that makes Tafamidis Meglumine Capsule. Other makers that haven’t reported a problem are shown in the green card below.

Availability of affected NDCs
From the FDA shortage report
1 NDCs
To be discontinued 1
Affected strengths still supplied
Among manufacturers reporting this shortage
0/1 strengths
No supply 1
FDA-reporting manufacturers with supply
Among manufacturers reporting this shortage
0/1 makers
No supply 1
Other manufacturers
We couldn’t automatically confirm other manufacturers of Tafamidis Meglumine Capsule that aren’t reporting a shortage. Ask your pharmacist whether a different manufacturer or strength can be ordered.
Shortage timeline
  1. Sep 29, 2025
    Currently in shortage
    1 of 1 product affected.
  2. Sep 29, 2025
    First reported to the FDA
    1 product first listed.

Built from FDA posting and update dates. The end date FDA publishes is the posting/update date, not a true resolution date, so durations are approximate.

What exactly is on backorder — by manufacturer

Manufacturer: Pfizer Inc. 📞 800-879-3477 1 NDC click to expand
Status NDC / product Strength Availability Related information Reason
To Be Discontinued Vyndaqel, Capsule, 20 mg soft gelatin capsules; blister card (120 total capsules) (NDC 0069-8730-30) NDC 00069-8730-30 Discontinuation of the manufacture of the drug upon exhausted supply/stop sale in December 2025.

These rows are manufacturer reports to the FDA for Tafamidis Meglumine Capsule — they do not necessarily cover every manufacturer that makes this drug. A company appears here only if it told the FDA it has a supply problem, so other makers may still have stock. That’s the basis for the Where else can I get Tafamidis Meglumine Capsule? options further down this page.

Why is Tafamidis Meglumine Capsule in shortage?

Pfizer has reported to the FDA that they are permanently stopping production of Vyndaqel 20 mg soft gelatin capsules, which come in a blister card of 120 capsules total (NDC 0069-8730-30). According to their report, they plan to sell through whatever supply is left and then fully stop sales in December 2025.

It's worth knowing that Pfizer did not give a specific public reason for why they made this decision — just that this particular product is being discontinued. This report covers only this specific Pfizer product and package size, so it doesn't necessarily mean tafamidis meglumine 20 mg capsules are gone from the market entirely, as other manufacturers may be listed separately on the shortage page.

Based on the manufacturer-reported reason(s) and notes on file with the FDA for Tafamidis Meglumine Capsule, summarized in plain English by HelloPharmacist. A drug can be short for more than one reason, and the FDA updates these as manufacturers report changes.

What should I do if I take Tafamidis Meglumine Capsule?

Tafamidis meglumine (Vyndaqel) 20 mg capsules are currently on the FDA drug-shortage list, so I want to walk you through what this means for you.

The affected product is the 20 mg soft gelatin capsule (120-capsule blister card). Right now there is no available source reported for this strength, and no other strength is listed as still in stock. This is the medicine you take, so I understand this news may feel unsettling.

Here is the reason behind it: the manufacturer, Pfizer, has reported this product as to be discontinued, with manufacturing ending once current supply is exhausted and a stop-sale planned for December 2025. Because this is a discontinuation rather than a temporary delay, the supply problem may be permanent. There is no recovery date to expect.

  • Do not stop, skip, or change your dose on your own.
  • Ask your pharmacy to check wholesalers and other manufacturers, since national data may not match local stock.
  • Because this product is being discontinued, talk with your prescriber soon about your next steps — they can discuss a clinician-chosen option that fits you.

Pfizer's contact number is listed on this page for reference, though your pharmacy usually handles those calls. This is general information and not individualized medical advice.

If you are a patient:
  • Don’t stop or change the medication on your own — talk to your prescriber first.
  • If this is part of an ongoing or essential regimen (for example HIV treatment or prevention, seizure, heart, transplant, diabetes or mental-health medicines), do not skip or ration doses — contact your pharmacist or prescriber right away to arrange continued supply before you run out.
  • Ask your pharmacy to check other manufacturers, strengths, package sizes, and nearby stores.
  • Ask your prescriber whether a different strength, formulation, or the brand/generic version is appropriate.
Keep reading
Our full Tafamidis guide

Uses, dosing, side effects, prices, and the complete FDA label — written in plain English and pharmacist-reviewed.

Read the Tafamidis guide →
Therapeutic equivalents & pricing 1 productclick to expand

Orange Book–rated equivalents of the affected strengths, with the latest NADAC price (a federal retail-acquisition benchmark, not your copay) and an evidence-based availability label. Cheapest first.

ProductManufacturerPackageNADAC $/unitAB ratingAvailability
Vyndamax 61 mgNDC 00069-8730-30 Pfizer 1 capsule FDA listed

Equivalents share the same ingredient, strength, dosage form and route; an AB rating means the FDA considers them substitutable. NADAC is a national retail-pharmacy acquisition benchmark from CMS — not what you pay. Availability is inferred from recent pricing, not a stock check.

Other drugs in the same treatment class

These are different medicines — not other versions of Tafamidis Meglumine Capsule — that fall in the same broad treatment class (protein stabilizers) . They are not automatic substitutes: they can differ in how they work, dosing, effectiveness, side effects and what they’re approved to treat. Do not switch on your own. This list is for information only — ask your prescriber or pharmacist whether any of them is appropriate for you.

Identity & classification

GCN Seq No 079710
GCN 46258
HICL code 045729
Ingredient (HICL) Tafamidis
HIC1 code P
Therapeutic class — broad (HIC1) Endocrine System
HIC2 code P9
Therapeutic class — intermediate (HIC2) Amyloidosis Agents
HIC3 code P9A
Therapeutic class — specific (HIC3) Protein Stabilizers
AHFS code 24:04.92.00
AHFS class Cardiac Drugs, Miscellaneous
FDB label name VYNDAMAX 61 MG CAPSULE
FDB brand name Vyndamax
Legend status F — Federal legend — prescription drug or device
GPI-1440550080000120
GPI classVyndamax
Where does this data come from?
Identity codes come from First Databank (FDB) (HICL ingredient, HIC1–3 therapeutic-class hierarchy, GCN, AHFS class, legend status) and Medi-Span GPI, mapped from a representative affected NDC. Licensed reference data — for identification only.

Other cardiovascular shortages

Tafamidis Meglumine Capsule shortage FAQs

Is Tafamidis Meglumine Capsule in shortage?
Yes — the FDA currently lists Tafamidis Meglumine Capsule in shortage (status: “To Be Discontinued”, first reported Sep 29, 2025). 1 of 1 product is affected. This is national, manufacturer-reported data, so your pharmacy may still have stock.
Which products are affected?
Vyndaqel, Capsule, 20 mg soft gelatin capsules; blister card (120 total capsules) (NDC 0069-8730-30) (NDC 00069-8730-30). The full per-NDC list (availability, manufacturer and status) is in the table above — each NDC links to its own page.
When will Tafamidis Meglumine Capsule be available again?
The manufacturer reports: Discontinuation of the manufacture of the drug upon exhausted supply/stop sale in December 2025. The FDA does not publish a single guaranteed restock date — confirm with your pharmacy.
What should I do if I take Tafamidis Meglumine Capsule?
Don’t stop or change it on your own. Ask your pharmacist whether they can order it from another manufacturer or a different strength/package size, and ask your prescriber about a long-term plan before your supply runs out.

Still have a question about the Tafamidis Meglumine Capsule shortage?

Ask a pharmacist about this shortage →
How to read the Supply-Risk rating
Low (1–2)Multiple manufacturers still supplying and most strengths or pack sizes sourceable.
Medium (3)Some constraint — fewer suppliers or a notable share of NDCs unavailable.
High (4–5)Down to a single source, most strengths or pack sizes unsourceable, or a long-running outage.
Where does this data come from?
Shortage records come from the FDA Drug Shortages Database API via openFDA (/drug/shortages) — drug, manufacturer & contact, NDC/product, status, availability, reason, therapeutic category and posting/update dates. Current / To Be Discontinued = active; Resolved is kept for history. The Supply-Risk rating is assessed per active ingredient and adds the FDA NDC Directory (still-marketed manufacturers by ingredient & form); same-medicine and equivalent products use First Databank classification + CMS NADAC pricing; Medicaid use + most-affected states come from CMS Medicaid State Drug Utilization Data. Reference only — confirm current status with the manufacturer or FDA before acting on it.
Data structure & sourcing designed and verified by Dr. Brian Staiger, PharmD.
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