When your compound presents specific production challenges, a systematic, solution-focused CDMO makes a world of difference.

Lannett CDMO is equipped to handle oral solid dose products: controlling for solubility, maintaining stability, and ensuring consistent bioavailability using documented approaches and analytical verification.
By simplifying complexity through scientific precision, we help bring challenging compounds to market with confidence.
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Accelerate Development with Lannett CDMO
- Streamlined development of oral solid dose formulations
- Extensive expertise and high-volume manufacturing
- Commitment to quality and regulatory compliance

Our track record speaks volumes
- 17 approved product applications since 2019
- 96% average product yield rate
- Zero critical FDA Form 483 observations

Learn More About Partnering with Lannett.

https://www.lannettcdmo.com/

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