Oral and respiratory contract manufacturing

Looking for a world-class cost competitive US based contract manufacturer?

Lean on Hikma. 

We offer a state-of-the-art 1million sq. ft. facility in Columbus, Ohio, USA. 

We can manufacture and package a broad range of high-quality dosage forms. 

Solid oral dose: tablets and capsules
Oral liquid solutions and suspensions
Multi and unit dose nasals
Dry powder inhalers

We can also manufacture and package potent compounds in our dedicated high containment operations (HCO) facility. 

We deliver at the speed you demand. Robust and collaborative tech transfer process. Agile, reliable and scalable commercial operations. 

We have an excellent compliance track record. FDA, EMA, AND DEA licensed. 

Zero critical observations in 20+ years. 

Best in class TRIR* safety performance (*total recordable incident rate)

Export to 80+ countries worldwide. 

We make your medicines just like we make our own.

So you can lean on us.

Solid, nasal and liquid dosage forms and dry powder inhaler technologies with high containment operations

Our focus

Step inside our all-encompassing and agile manufacturing facility, and you’ll see we can efficiently deliver a range of high-quality, cost-competitive dosage forms and devices to meet your demands and deadlines. Our expansive, centrally located DEA/FDA/EMA-licensed facility has supported 80+ different countries, with weekly management of international exports.

We are 100% dedicated to making your medicines like they are our very own. It’s why our cutting-edge German-designed, brand-built manufacturing facility was created to be dual-capacity, with integrated systems dedicated to both our Hikma labelled products and CMO. The result: Same expert teams. Same precision processes. Same high-quality products.

We’re laser-focused on delivering agility, reliability and scalability. In under 24 months, our highly-trained Columbus, Ohio team recently brought to market a critical life-saving device using our effective, robust, and rapid-tech transfer process.

When you partner with us, you’re accessing the same state-of-the-art 1,000,000 sq. ft facility on 80 acres that the FDA has repeatedly used as a training site for qualifying new inspectors within their organization. With zero critical FDA observations for two decades, and best-in-class TRIR safety performance, you can lean on us for all your Generics CMO needs.

Get in touch

Contact us to discuss your oral, nasal and respiratory CMO needs.

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