International Supply Chains: Why Dependence on Foreign Manufacturing Is Causing Drug Shortages in 2026

3January
International Supply Chains: Why Dependence on Foreign Manufacturing Is Causing Drug Shortages in 2026

When you walk into a pharmacy and your prescription isn’t in stock, it’s not because the doctor got it wrong. It’s because the pill you need was made halfway across the world - and something broke along the way.

How a Pill Made in China Ends Up Missing on Your Shelf

More than 80% of the active ingredients in U.S. prescription drugs come from abroad, mostly from China and India. These aren’t just minor components - they’re the actual chemicals that make the medicine work. For example, the generic antibiotic amoxicillin, used by millions every year, relies on raw materials sourced almost entirely from two provinces in China. When a factory there shuts down for environmental checks, or a port in Shanghai gets backed up, the ripple effect hits U.S. hospitals within weeks.

It’s not just about distance. It’s about concentration. The global pharmaceutical supply chain is built on efficiency, not safety. Companies moved production overseas because labor was cheaper, regulations looser, and taxes lower. In 2020, the U.S. imported $12.4 billion worth of active pharmaceutical ingredients (APIs) from China alone. Today, that number is still rising. But the system doesn’t have room for error. One factory outage can delay production for hundreds of millions of doses.

Why Resilience Was Ignored for Cost Savings

For years, drugmakers treated supply chains like a spreadsheet line item. Why keep a factory in Ohio when you can make the same ingredient in Hyderabad for 60% less? It made sense - until it didn’t.

During the pandemic, the world saw what happens when you bet everything on one region. When China locked down in early 2020, the U.S. ran out of heparin, a blood thinner. When India restricted exports of generic drugs in 2022 to protect its own supply, hospitals scrambled to find alternatives for antibiotics and heart medications. The result? 228 drug shortages in the U.S. in 2024 - the highest number in a decade, according to the FDA.

The problem isn’t just politics or pandemics. It’s structural. Most drug manufacturers don’t own the factories that make their active ingredients. They outsource them to contract manufacturers - often in countries with weak oversight. A single supplier might serve 15 different U.S. brands. If that supplier runs into trouble, everyone’s out of stock.

What’s Being Done - And Why It’s Not Enough

The U.S. government has tried to fix this. The 2022 CHIPS and Science Act included $1.5 billion to bring API production back home. In 2024, the FDA launched a program to fast-track approval for domestic API manufacturers. But building a chemical plant isn’t like building a smartphone factory. It takes 3-5 years. And the cost? Up to $500 million per facility.

Some companies are trying to diversify. A few large pharma firms now source APIs from both India and Vietnam, with backup suppliers in Poland and Ireland. One major insulin maker doubled its supplier base in 2023 and saw its stockout rate drop by 40%. But these are exceptions. Most small and mid-sized drugmakers still rely on single-source suppliers because switching is expensive and risky.

Even when companies try to reshore, they hit walls. The U.S. doesn’t have enough trained chemical engineers to run these plants. Skilled workers in this field are aging out, and few new graduates are choosing pharma manufacturing. That’s why 33% of companies report understaffing in global trade and production roles - a problem that won’t fix itself overnight.

A pharmacist holding a single pill bottle as factories in China and India fade into darkness behind her.

The Hidden Cost: Tariffs, Delays, and Rising Prices

Tariffs have made things worse. Since 2024, the U.S. has added 12 new tariff categories targeting pharmaceutical inputs. One of them hit a key chemical used in blood pressure meds - raising its price by 270%. That cost didn’t disappear. It got passed on to insurers, then to patients.

Shipping times have also ballooned. In 2019, it took 14 days for a container of APIs to get from China to Los Angeles. Today, it’s 21 days - and that’s if nothing goes wrong. Delays of 30-60 days are now common during monsoon season in India or port strikes in Europe. For drugs with short shelf lives - like insulin or vaccines - that’s a death sentence.

Meanwhile, the cost of keeping extra stock - called “just-in-case” inventory - has jumped 15% since 2022. Some hospitals are now storing six months’ worth of critical drugs. But that’s not sustainable. Storage costs money. And if the drug expires before it’s used? It’s thrown away. The FDA estimates $1.2 billion in wasted medications annually due to supply chain instability.

Real Solutions Are Already Working - But Rare

There are success stories. One U.S.-based generic drugmaker, based in North Carolina, switched from relying on China to using dual sourcing: 60% from India, 40% from a new partner in Portugal. They also invested in a digital twin system - a virtual model of their entire supply chain - that alerts them to delays before they happen. Their on-time delivery rate is now 99.2%. They didn’t get rich doing it. But they didn’t run out of stock either.

Another company, a small manufacturer of asthma inhalers, started using microfactories - automated, compact production units that can be set up quickly in the U.S. or Mexico. These cost 40% more upfront, but they cut lead times by 25%. They now make 30% of their product locally and have eliminated all shortages in the past 18 months.

Blockchain is helping too. Some suppliers now use it to track every batch of API from raw material to final pill. If a batch fails quality tests, they can trace it back to the exact batch of chemicals - and isolate the problem. This cuts quality disputes by 65% and reduces recalls.

But these are still niche. Only 40% of Asian-based manufacturers have adopted multi-shoring strategies. Most still operate on the old model: lowest cost wins. And until that changes, shortages will keep happening.

A small U.S. microfactory glows with digital supply chain data, surrounded by children planting trees of resilience.

What This Means for You

You might not think about where your pills come from. But when your medication is suddenly unavailable, it’s not just inconvenient - it’s dangerous. Missing a dose of blood thinners, epilepsy meds, or insulin can lead to hospitalization - or worse.

If you’re on a long-term prescription, ask your pharmacist: Is this made in the U.S.? If not, ask if there’s an alternative with a more reliable supply chain. Some generics have the same active ingredient but come from different manufacturers. Your doctor can switch you - if they know to ask.

You can also support policy changes. Contact your representative. Ask them to support bills that fund domestic API production and require drugmakers to disclose where their ingredients come from. Transparency is the first step toward accountability.

The Road Ahead

The global pharmaceutical supply chain isn’t going away. But it’s changing. By 2027, experts predict that 50% of major drugmakers will have moved from single-source to multi-shoring models. AI-driven forecasting will help predict shortages before they happen. Governments will likely mandate minimum stockpiles for critical drugs.

But none of this matters if we don’t change the mindset that cheap is always better. The cost of a drug shortage isn’t just financial. It’s measured in lives. In missed treatments. In ER visits. In preventable deaths.

The pills we depend on aren’t just products. They’re lifelines. And right now, that lifeline is hanging by a thread - stretched across oceans, held together by fragile factories and outdated systems.

It’s time to rebuild it - not for profit, but for people.

Why are drug shortages happening now?

Drug shortages are happening now because the global supply chain for active pharmaceutical ingredients (APIs) is overly concentrated in just a few countries - mainly China and India. These regions produce over 80% of the world’s drug ingredients. When a factory shuts down, a port closes, or a government restricts exports, the entire chain breaks. Unlike consumer goods, drugs can’t be easily swapped out. There’s no backup supplier ready to jump in, and building new facilities takes years. In 2024, the U.S. had 228 drug shortages - the highest in a decade - directly tied to these supply chain vulnerabilities.

Can the U.S. make its own drugs again?

Yes, but it’s expensive and slow. The U.S. has the technical ability to produce APIs domestically, but it lacks the infrastructure and workforce. Building a single API manufacturing plant costs between $300 million and $500 million and takes 3-5 years. There’s also a shortage of trained chemical engineers and technicians. While the government has pledged $1.5 billion to bring production home, that’s only enough to support a handful of new facilities. Without major investment in workforce training and incentives for private companies, domestic production will remain a small fraction of total supply.

Are generic drugs more vulnerable to shortages?

Yes, generics are far more vulnerable. Brand-name drugs often have multiple suppliers and higher profit margins, so companies invest in backup production. Generic manufacturers operate on razor-thin margins - sometimes just pennies per pill. To stay profitable, they rely on the cheapest source, often a single factory in China or India. If that factory has a problem, there’s no alternative. In fact, 85% of all drug shortages in 2024 were for generic medications. These are the drugs most people depend on - and the ones most likely to disappear.

What can I do if my medication is out of stock?

First, don’t stop taking your medication without talking to your doctor. Ask your pharmacist if there’s a different brand or manufacturer of the same drug available - sometimes the active ingredient is identical, but it comes from a different supplier. If not, your doctor can often prescribe an alternative with a similar effect. You can also check the FDA’s Drug Shortages database for updates. And if this happens often, consider asking your doctor to switch you to a drug with a more reliable supply chain - even if it’s slightly more expensive. Your health is worth it.

Is nearshoring to Mexico a real solution?

Yes, but with limits. Nearshoring to Mexico cuts shipping time by 30-40% compared to Asia and avoids many of the geopolitical risks tied to China. Some U.S. drugmakers are already moving API production there, especially for injectables and oral solids. Labor costs are higher than in Asia, but lower than in the U.S., and proximity allows for faster response to demand changes. However, Mexico’s chemical manufacturing capacity is still limited. It can’t replace China for bulk production of complex APIs. It’s best used as a backup - not a full replacement.

How do tariffs affect drug availability?

Tariffs make drugs scarcer and more expensive. Since 2024, the U.S. has imposed new tariffs on over $340 billion in imports - including key chemicals used in blood pressure, diabetes, and heart medications. These tariffs raise the cost of raw materials by 20-270%. Instead of absorbing the cost, manufacturers pass it on to patients and insurers. Some companies stop importing those ingredients altogether, leading to shortages. Others raise prices. Either way, patients pay the price. The irony? Tariffs meant to protect U.S. industry are making essential medicines harder to get.

Will AI help fix drug supply chains?

AI is already helping - but only in advanced companies. AI can predict delays by analyzing shipping data, weather patterns, customs clearance times, and factory output. Some firms now use digital twins - virtual models of their entire supply chain - to simulate disruptions before they happen. These tools can cut lead times by 20% and reduce stockouts by up to 30%. But adoption is low. Only 68% of large pharma companies use AI in their supply chains, and smaller ones can’t afford it. Without widespread access, AI won’t fix the system - it’ll just widen the gap between big and small players.

Comments

Oluwapelumi Yakubu
Oluwapelumi Yakubu

Look, we’ve been dancing around the elephant in the room: capitalism doesn’t care if you live or die-it cares about margins. We outsourced our pharmaceutical soul for a few pennies per pill, and now we’re surprised when the lifeboat sinks? This isn’t a supply chain crisis-it’s a moral collapse dressed in balance sheets.

We treat medicine like fast fashion: cheap, disposable, replaceable. But a human body doesn’t run on TikTok trends. When your insulin vanishes, it’s not a ‘logistical hiccup’-it’s a death sentence with a barcode.

And yet, we keep voting for the same people who cheerlead offshoring while sipping artisanal cold brew in their DC condos. The system isn’t broken-it’s working exactly as designed. For someone else.

Reshoring? Great. But without universal healthcare, it’s just rearranging deck chairs on the Titanic while the water rises. We need to stop pretending this is about efficiency. It’s about who we are-and who we’re willing to let die to keep our profits clean.

January 3, 2026 at 12:35

en Max
en Max

It is important to note, however, that the structural vulnerabilities in the global pharmaceutical supply chain are not merely the result of offshoring; they are exacerbated by systemic underinvestment in domestic manufacturing infrastructure, coupled with regulatory fragmentation across federal agencies. The FDA’s approval timelines, while streamlined in certain initiatives, remain incompatible with the capital-intensive, highly regulated nature of API production.

Moreover, the labor gap-particularly in chemical engineering and GMP compliance-is not a transient issue; it is the cumulative effect of decades of disinvestment in vocational STEM pathways. Without a coordinated, multi-generational workforce development strategy-anchored in community colleges, apprenticeships, and federal subsidies for plant operators-the resiliency narrative remains aspirational, not actionable.

Furthermore, the economic disincentives for multi-sourcing are non-trivial: switching suppliers requires re-validation, re-qualification, and re-licensing under 21 CFR Part 211, which can add 18–24 months and $2–4M in non-recoverable costs per product line. Thus, while diversification is ideal, it is not economically rational for margin-constrained generic manufacturers.

January 5, 2026 at 00:51

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