Economic Impact of Patent Expiration: How Drug Prices Drop After Patents Expire

Economic Impact of Patent Expiration: How Drug Prices Drop After Patents Expire

When a drug’s patent runs out, something powerful happens: prices don’t just dip-they plummet. For patients paying hundreds of dollars a month for a brand-name medication, that moment can mean switching from a $850 prescription to a $10 generic. It’s not magic. It’s economics. And it’s happening right now with drugs like Eliquis, Humira, and Ozempic.

What happens when a patent expires?

A pharmaceutical patent gives a company exclusive rights to sell a drug for about 20 years. During that time, they’re the only one who can make it. That means they set the price-no competition, no pressure. But once the patent expires, other companies can legally produce identical versions called generics. And that’s when the real price drop begins.

The first generic to enter the market usually cuts the price by 15% to 20%. That’s noticeable, but not dramatic. Then comes the second. Then the third. By the time five or six companies are selling the same drug, prices can drop 70% or more. In the U.S., after eight years, some drugs lose over 80% of their original price. A 2023 study in JAMA Health Forum found that for 505 drugs analyzed, the average price fell 82% over eight years after patent expiration.

It’s not just about more companies. It’s about competition. When there’s only one seller, they can charge what they want. When there are 10, they’re fighting for shelf space, for pharmacy contracts, for patient trust. That’s when prices really start to slide.

Why do some drugs drop faster than others?

Not all drugs are created equal. Small molecule drugs-like blood thinners, statins, or antidepressants-are relatively easy to copy. Their chemical structure is simple to replicate. That’s why drugs like Lipitor and Plavix saw massive price drops within months of patent expiration.

But complex drugs, especially biologics like Humira or Enbrel, are different. These aren’t just pills. They’re made from living cells. Copying them isn’t as simple as mixing chemicals. The copies are called biosimilars, and they take longer to develop, test, and get approved. That’s why Humira’s patent expired in 2016, but the first biosimilar didn’t hit the market until 2023.

Even then, the price didn’t crash right away. AbbVie, the maker of Humira, filed over 130 secondary patents on minor changes-delivery devices, dosing schedules, formulations. These didn’t make the drug better, but they delayed competitors. It’s called a “patent thicket,” and it’s a common tactic. The R Street Institute found that 78% of new patents filed between 2010 and 2020 weren’t for new drugs-they were for old ones with small tweaks.

Why do prices vary so much between countries?

The same drug can drop 82% in the U.S. but only 18% in Switzerland. Why? It comes down to how each country handles drug pricing.

In the U.S., there’s no central price negotiation. Pharmacies, insurers, and PBMs (pharmacy benefit managers) all negotiate separately. That creates a messy, fragmented system. When generics enter, some payers jump on the lower price. Others stick with the brand because of rebates or contracts. That’s why patients sometimes see a big drop, but their insurance still pays a lot.

In Europe, governments set price caps. They negotiate bulk deals. If a generic comes in at half the price, they just switch the official reimbursement rate. That’s why countries like the UK and Germany saw 60%+ price drops within a few years.

Australia uses a reference pricing system: if a drug’s price falls in one country, they match it. That creates a domino effect. Switzerland, on the other hand, has strict rules limiting how low prices can go-even with competition.

Who benefits when prices drop?

Patients. Insurers. Medicare. Medicaid. Taxpayers. Everyone who pays for healthcare.

A 2023 Kaiser Family Foundation survey found that 68% of insured adults saw lower out-of-pocket costs when generics became available. For someone taking Eliquis (apixaban), that meant going from $850 a month to $10. That’s not a savings-it’s a lifeline.

Medicare Part D saved $11 billion in 2023 just from generic and biosimilar use. The Congressional Budget Office estimates that over the next decade, generic and biosimilar competition will save the U.S. healthcare system $1.7 trillion.

But here’s the catch: not everyone feels it right away. Even when generics are available, insurance formularies can delay access. Some plans require patients to try the brand first. Others don’t cover the generic unless the doctor writes “dispense as written” on the prescription. Pharmacists can’t substitute unless the law allows it-and rules vary by state.

What’s holding back faster price drops?

The biggest barrier isn’t science. It’s strategy.

Originator companies know their profits will vanish once generics arrive. So they fight to delay them. Tactics include:

  • Patent thickets: Filing dozens of minor patents to block competitors.
  • Pay-for-delay deals: Paying generic makers to wait before launching.
  • Restrictive contracts: Forcing insurers to favor the brand in exchange for rebates.
  • Complex manufacturing: Making biosimilars expensive and slow to produce.
Take semaglutide (Ozempic, Wegovy). The base patent expires in 2026. But the manufacturer has filed 142 patents covering delivery pens, dosing regimens, and combination therapies. Experts say these could delay real competition until 2036.

The FDA approved 870 generic drugs in 2023-up 12% from 2022. But for complex drugs, approval can take over two years. And each bioequivalence study costs $2-5 million. That’s a high barrier for small generic companies.

A tangled thicket of legal patents blocks a small generic drug maker trying to enter the market.

What’s changing now?

Regulators are starting to push back.

In 2023, the U.S. Patent Office tightened rules on patent thickets. The European Commission proposed limits on supplementary protection certificates. The Inflation Reduction Act lets Medicare negotiate prices for some drugs-something that’s forcing manufacturers to rethink their timelines.

The European Medicines Agency now wants biosimilars to reach 70% market share within three years of patent expiry. Right now, it’s around 45%. They’re pushing for faster approvals and mandatory substitution rules.

Meanwhile, generic drugmakers are investing more in complex drugs. Companies like Amgen and Sandoz are building labs to copy biologics. In 2023, the global generic drug market hit $407 billion. It’s expected to hit $700 billion by 2030.

What does this mean for you?

If you’re on a brand-name drug with an expiring patent, ask your doctor or pharmacist: “Is there a generic or biosimilar available?” Don’t assume your insurance will automatically switch you. Check your formulary. Ask if you can switch to the cheaper version.

If you’re paying cash, call local pharmacies. Some generics cost less than a coffee. One patient on Reddit reported paying $12 for a 30-day supply of generic metformin-down from $180 for the brand.

And if you’re watching a drug like Ozempic or Humira stay expensive even after patent expiration, understand why: it’s not about the science. It’s about contracts, rebates, and legal loopholes. The system works-when it’s not being gamed.

The bottom line? Patent expiration is the most powerful tool we have to lower drug prices. But it only works if the system doesn’t block it.

How long until a generic hits the market?

It varies. For simple pills: 6 to 18 months after patent expiry. For complex biologics: 3 to 7 years. In the U.S., the average time from patent expiry to first generic is 30 months. In Europe, it’s 12 to 18 months.

Do all drugs get generics?

No. Some drugs are too complex to copy easily. Others have such small markets that no company finds it worth the cost. But for the top 100 most-prescribed drugs, 95% have generic versions available within five years of patent expiry.

A U.S. pharmacy chaos contrasts with a calm European pharmacy where generics are easily available.

Why don’t all pharmacies stock the cheapest generic?

Many pharmacies are locked into contracts with pharmacy benefit managers (PBMs) that pay them more to stock the brand-name drug-even if it’s more expensive. That’s why you might see a $10 generic on the shelf, but your pharmacy says they can’t give it to you without a special request.

Can I ask my doctor to prescribe a generic?

Yes. Always. In fact, in 49 U.S. states, pharmacists can automatically substitute a generic unless the doctor writes “dispense as written.” Ask your doctor to write “generic acceptable” on the prescription.

Do biosimilars work as well as the original?

Yes. The FDA requires biosimilars to show no clinically meaningful difference in safety or effectiveness. Millions of patients have switched from Humira to Amjevita or Cyltezo with no issues. The main difference is cost-not quality.

Will drug prices go back up after generics enter?

Rarely. Once generics are in place, prices rarely rise again. Even if one manufacturer leaves the market, others fill the gap. The only exception is if a drug is discontinued due to supply issues-but that’s not about price. It’s about production.