Pfizer’s Capsugel Fetches $2.375 Billion - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe

Pfizer’s Capsugel Fetches $2.375 Billion


ePT--the Electronic Newsletter of Pharmaceutical Technology

After completing a strategic review of options for its Capsugel business, Pfizer announced on Apr. 04, 2011 that Kohlberg Kravis Roberts & Co L.P  (KKR )agreed to acquire the pharmaceutical and dietary capsule company.

Capsugel generated approximately $750 million in revenue and manufactured more than 180 billion capsules in 2010. According to Guido Driesen, president and general manager of Capsugel, the transaction is “an endorsement of Capsugel’s consistent success to date and its potential for future growth…”

But it also represents Pfizer’s previously announced objectives to streamline its business. Pfizer gained Capsugel in 2000, as part of its $90-billion acquisition of Warner-Lambert, which took over original owner, Parke-Davis, in the 1970s.

KKR co-founders and co-CEOs, Henry Kravis and George Roberts, stated in a Pfizer Apr. 4, 2011 press release that: “Capsugel has an excellent portfolio and outstanding reputation for providing high-quality, innovative drug-delivery solutions.” They also shared Capsugel’s enthusiasm for future potential. KKR has a current private equity portfolio that includes over 60 companies, over $210 billion in annual revenues and more than 900,000 employees.

Pfizer stated that Capsugel will maintain its global headquarters in New Jersey and that any Pfizer staff dedicated to the business would be transferred to Capsugel under the leadership of Guido Driesen.

The sale will enable Pfizer to increase the previously announced $5 billion it plans to spend on the repurchase of its common shares on the open market in 2011. The transaction is expected to close in the third quarter, subject to regulatory and closing requirements.

ADVERTISEMENT

blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
How does your company apply quality-by-design (QbD) principles to manufacturing processes?
To all processes for both new and legacy products
To all process for new products only
To select process for new products only
To select processes for both new and legacy products
Do not use QbD
To all processes for both new and legacy products
22%
To all process for new products only
12%
To select process for new products only
20%
To select processes for both new and legacy products
22%
Do not use QbD
24%
View Results
UPCOMING CONFERENCES

Programs for Investigational and Pre-Launch Drugs
Philadelphia, PA
July 17-18, 2013
Request Brochure

Strategic Pipeline Planning & Portfolio Valuation
Philadelphia, PA
August 13-14, 2013
Request Brochure

MES 2013 - Forum on Manufacturing Execution Systems
Philadelphia, PA
August 14-15, 2013
Request Brochure

Mobile Innovation for the Life Sciences Industry
Philadelphia, PA
August 20-21, 2013
Request Brochure

See All Conferences >>

Eric Langer Outsourcing Outlook Eric LangerOutsourcing's Modest Role as a Cost-Containment Strategy
Patricia Van Arnum Ingredients Insider Patricia Van ArnumIntellectual Property Battles in Solid-State Chemistry
Nathan Jessop Industry Insider Nathan Jessop Campaign Against Counterfeit Drugs Continues
Lynn Torbeck Statistical Solutions Lynn D. TorbeckCompositing Samples and the Risk to Product Quality
 More
Inadequate Access to Medicines Puts EU at Risk
FDA Offers Insight on QbD for Modified-Release Products
Global Biosimilars Market to Reach $2.445 Billion in 2013
Adapting to Change
AstraZeneca and Exco InTouch Collaborate to Augment Current COPD Pathways
FindPharma Custom Search
Source: ePT--the Electronic Newsletter of Pharmaceutical Technology,
Click here