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Pramlintide Acetate Injection (SymlinPen 120, SymlinPen 60) shortage

Possibly permanent — AstraZeneca AB, the only company we could find that sells pramlintide acetate injections, has told the FDA it is discontinuing its product as of Oct 6, 2026. The FDA lists this under “To be discontinued”. We could not find another company that sells the same medicine, so talk with your prescriber about a long-term plan before your supply runs out.

To Be Discontinued ⚠ Supply risk: High Endocrinology/Metabolism 2 products 345 days First posted Oct 27, 2025 Updated Oct 27, 2025
Here’s the bottom line

AstraZeneca is stopping production of Symlin (pramlintide acetate) injection, and this change may be permanent. No other manufacturers are listed as a source for this medicine right now.

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 medicine? See the ‘What to do’ note from Dr. Brian Staiger, PharmD →
2
Affected NDCs
0/1
Reporting makers with supply
0/1
Affected strengths still listed
345
Days on the list
39
Medicaid Rx (2026)
Source: FDA Drug Shortages Database API (openFDA). Last refreshed Oct 6, 2026 · yesterday

Is pramlintide acetate still in shortage? — status as of Oct 6, 2026

Still listed as “To be discontinued” as of Oct 6, 2026. We could not find another company that sells pramlintide acetate injections, so this may become permanent. Talk with your prescriber about a long-term plan before your supply runs out.

⚠ Supply risk: High 5 of 5 risk factors
  1. Every strength is still listed by a company — 0 of 1 strength
  2. More than one company still lists it — 0 of 1 reporting company with supply
  3. Most affected NDCs still available — none listing supply
  4. Not a long-running shortage — 344 days (a discontinuation notice, not an outage)
  5. Listed by several companies — 1 company (1 reporting)

A rule-based estimate of national supply risk, counting both the companies reporting the shortage and the companies listing the same medicine without a report — never your local pharmacy’s stock. How the rating works.

The charts count only the companies that reported this shortage to the FDA; we could not confirm another company listing it (see below).

Availability of affected NDCs
From the FDA shortage report
2 NDCs
To be discontinued 2
Affected strengths still listed by a company
A company on the shortage report with supply, or another company selling that strength
0/1 strengths
No company found making it 1
Reporting companies with supply
Among the 1 company that reported this shortage
0/1 reporting
Reporting no supply 1
Other companies
We couldn’t confirm another company listing Pramlintide Acetate Injection in the FDA NDC Directory without a shortage report. Ask your pharmacist whether a different company’s version or another strength can be ordered.
Shortage timeline
  1. Oct 27, 2025
    Currently in shortage
    2 of 2 products affected.
  2. Oct 27, 2025
    First reported to the FDA
    2 products 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.

Which pramlintide acetate products are affected — by company

Company: AstraZeneca AB 📞 800-236-9933 2 NDCS click to expand
Status NDC / product Strength Availability Related information Reason
To Be Discontinued SymlinPen® 60 Injection, 1000 ug/mL NDC 00310-6615-02 1000 ug/mL — Discontinuation of the manufacture of the drug. —
To Be Discontinued SymlinPen® 120 Injection, 1000 ug/mL NDC 00310-6627-02 1000 ug/mL — Discontinuation of the manufacture of the drug. —

These rows are company reports to the FDA for Pramlintide Acetate Injection — they do not cover every company that lists this medicine. A company appears here only if it told the FDA it has a supply problem, so other companies may still have stock.

Why is AstraZeneca AB discontinuing pramlintide acetate?

A note from Dr. Brian Staiger, PharmD · Written Oct 3, 2026

AstraZeneca AB has reported to the FDA that it is permanently stopping the manufacture of two of its pramlintide acetate injection products — the SymlinPen® 60 and the SymlinPen® 120, both in the 1000 mcg/1 mL strength. That's why these specific products appear on the shortage list.

AstraZeneca did not share a specific public reason for why they are stopping production of these two pens. It's worth knowing that this report reflects only what AstraZeneca AB has filed with the FDA — it speaks only to their products and their decision, not to what other manufacturers may or may not have available.

Based on the company-reported reason(s) and notes on file with the FDA for Pramlintide Acetate Injection, summarized in plain English by HelloPharmacist. A drug can be short for more than one reason, and the FDA updates these as companies report changes.

What should I do if I take pramlintide acetate?

A note from Dr. Brian Staiger, PharmD · Written Oct 3, 2026

Pramlintide Acetate Injection (the SymlinPen pen) is currently on the FDA shortage list, and I want to walk you through what that means for you.

The one strength on this record, 1000 ug/1 mL — covering both SymlinPen 60 and SymlinPen 120 — has no available source reported right now. There is no other strength listed that still has supply.

The reason given is that the manufacturer, AstraZeneca, is discontinuing production of this medicine. Because this is a discontinuation rather than a temporary delay, this supply problem may be permanent, and no estimated-recovery date is listed. At this time, no other maker of this exact medicine appears in our records.

Here is what I suggest you do:

  • Do not stop, skip, or change your doses on your own — keep taking it as prescribed while you sort out next steps.
  • Since this product is being discontinued, please talk with your prescriber or pharmacist soon about a clinician-chosen plan going forward.
  • Manufacturer contact information is listed on this page for reference, though pharmacies usually handle those calls.

This information comes from national, manufacturer-reported FDA data and may not match your local pharmacy's actual stock. Your prescriber can help you find the right path for your situation.

Quick checklist for the pharmacy counter:
  • Ask your pharmacy to check other companies’ versions, other strengths, package sizes, and nearby stores.
  • If this is part of an ongoing or essential regimen (for example HIV, seizure, heart, transplant, diabetes or mental-health medicines), arrange continued supply before you run out rather than rationing doses.
Keep reading
Our full Pramlintide Injection guide

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

Read the Pramlintide Injection guide →
Therapeutic equivalents & pricing 2 productsclick 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
SymlinPen 1000 ug/mLNDC 00310-6627-02 AstraZeneca 2 cartridges $217.521 save 34% — Availability likely
SymlinPen 1000 ug/mLNDC 00310-6615-02 AstraZeneca 2 cartridges $330.952 — Availability likely

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.

Codes & classification for pharmacists and billers
GCN Seq No 063804
GCN 99514
HICL code 032805
Ingredient (HICL) Pramlintide Acetate
HIC1 code C
Therapeutic class — broad (HIC1) Electrolyte Balance/Metabolism/Nutrition
HIC2 code C4
Therapeutic class — intermediate (HIC2) Antihyperglycemics
HIC3 code C4H
Therapeutic class — specific (HIC3) Antihyperglycemic, Amylin Analog-Type
AHFS code 68:20.03.00
AHFS class Amylinomimetics
FDB label name SYMLINPEN 60 PEN INJECTOR
FDB brand name Symlinpen 60
Legend status F — Federal legend — prescription drug or device
GPI-142715005010D220
GPI classSymlinPen 60
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 endocrinology/metabolism shortages

Pramlintide acetate shortage FAQs

Is pramlintide acetate still in shortage?
Yes, and it may be permanent — AstraZeneca AB, the only company we could find that sells pramlintide acetate injections, has told the FDA it is discontinuing its product (FDA status as of Oct 6, 2026). Talk with your prescriber about a long-term plan before your supply runs out.
Which strengths of pramlintide acetate are affected?
The FDA record covers 1 strength: 1000 ug/mL. Right now we could not find any company still making it: the companies that reported the shortage say they are out, and no other company we found sells it. Ask your pharmacist and prescriber about options before you run out.
Which pramlintide acetate products are affected?
SymlinPen® 60 Injection, 1000 ug/mL (NDC 00310-6615-02); SymlinPen® 120 Injection, 1000 ug/mL (NDC 00310-6627-02). The full per-NDC list (availability, company and status) is in the table above — each NDC links to its own page.
When will pramlintide acetate be available again?
A discontinuation is usually permanent for that company’s product. We could not find another company that sells it, so ask your prescriber about a long-term plan and your pharmacy what it can still order.
Is the brand or the generic affected?
Only the brand (SymlinPen 120 and SymlinPen 60) is on this FDA record; it lists no generic pramlintide acetate injections. Availability can still differ between companies and package sizes — check the per-NDC table and confirm with your pharmacy.
What should I do if I take pramlintide acetate?
Don’t stop or change it on your own. Ask your pharmacist whether they can order it from another company or a different strength or package size, and ask your prescriber about a long-term plan before your supply runs out.

Still have a question about the pramlintide acetate shortage?

Ask a pharmacist about this shortage →
How to read the Supply-Risk rating
Low (0–2)Several companies still list it and most strengths or pack sizes are still listed by someone — counting both the companies reporting the shortage and the companies listing the same medicine without a report. A listing is not a stock check.
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 without a source, or a long-running outage. A company’s discontinuation notice is not an 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 (companies listing the same ingredient & form — the "other companies" the rating counts); 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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