News|Articles|August 31, 2021

Catalent Acquires Nutraceutical for $1 Billion

Catalent’s acquisition of Bettera paves the way for growth in the softgel and oral dose formulation and manufacturing market for nutraceuticals.

Catalent has reached an agreement to acquire Bettera Holdings for $1 billion, according to a company press release from Aug. 30, 2021. Bettera Holdings is a manufacturer specializing in the production of gummy, soft chew, and lozenge nutritional supplements.

This acquisition will complement Catalent’s existing softgel and oral dose formulation and manufacturing services. It will expand Catalent’s current consumer health technology platform with a wider range of technologies and ready-to-market product libraries, as well as a variety of packaging options to meet customers’ branding needs.

The acquisition is expected to close in 2021. As part of the deal, Catalent will acquire approximately 500 employees from Bettera, as well as their production facilities in California, Indiana, New Jersey, and Virginia.

“This acquisition allows us to significantly accelerate the growth of our consumer health business and offer customers access to the substantial potential in gummies, soft chews, and lozenges, which are experiencing double-digit growth,” said Aris Gennadios, president of Softgel and Oral Technologies at Catalent, in the press release. “This acquisition is a key strategic move for Catalent’s Consumer Health business, where our leadership in manufacturing technologies and formulation can offer customers more product development opportunities, and add manufacturing capacity in this dynamic and fast-growing segment.”

Source: Catalent


Related to this article

PharmTech Weekly Roundup—October 2, 2026
This week on PharmTech, Merck diversified its pipeline, USP emphasizes supply chain security, AI systems are examined, and speakers preview their presentations at CPHI Milan and AAPS PharmSci 360.
CPHI Milan 2026: Nitrosamine Risk Mitigation, Part 1
Capsugel's Bram Baert and Sandrine Picco argue that chasing zero nitrite in pharmaceutical excipients is often impractical and costly. They recommend setting scientifically justified, risk-based limits and consistently staying below them.
Regulatory Roundup—September 2026
The FDA opened an expedited IND pilot, tightened scrutiny of foreign trial data, and finalized a rule recognizing non-animal testing methods. In Europe, the EMA advanced pharmaceutical legislation reform, restricted 2 legacy products, and opened an injectable-iron safety review.