Perrigo Company may not be a household name, but nevertheless life is exciting for a medium-sized company in the pharmaceuticals world. Undeterred by a pending FDA warning letter about its Michigan facility, Perrigo recently entered into a definitive agreement to take over Paddock Laboratories in a cash deal worth Euros 394 million.
Perrigo buys Paddock for US$540 million
Home/Pharma News
|
Posted 04/03/2011
0
Post your comment

Perrigo develops, manufactures, and distributes OTC and prescription pharmaceuticals, nutritional products, active pharmaceutical ingredients and consumer products. It recorded net sales of US$2.7 billion in 2010 (Euros 1.95 billion), up 13.1% on 2009.
Paddock is a privately owned, Minneapolis-based company that focuses on the manufacturing and marketing of generic prescription specialty products. Manufacturing expertise encompasses a wide variety of dosage forms, including all types of semi-solids, liquids, powders, tablets, and capsules. The transaction is expected to close in the fourth quarter of its 2011 tax year, pending regulatory approval. The payment will be made over 15 years, for tax reasons.
Paddock brings with it a portfolio of 35 major marketed products, 20 products in development and approximately 25 Abbreviated New Drug Applications (ANDAs)* pending approval with the FDA. The acquisition is expected to expand Perrigo’s generic prescriptions business, particularly through its extended range of topical creams and gels, which fit nicely with Perrigo’s existing business.
The transaction is expected to increase Perrigo’s revenue by over US$200 million in its 2012 tax year. “This acquisition is an important next step forward in executing our strategy to expand our specialty portfolio of generic Rx products”, stated Mr Joseph C Papa, Perrigo Chairman and CEO. “It adds incremental scale, as well as excellent development and manufacturing capabilities across a spectrum of niche dosage forms”.
Business comments on the deal were mixed; nevertheless Perrigo’s share price was boosted on 25 January 2010, a few days after the deal was announced.
* An ANDA is an application for a US generic drug approval for an existing licensed medication or approved drug.
Related article
Source: Genetic Engineering and Biotechnology News, Zachs
Guidelines
Advances in EMA plans to streamline biosimilar assessment
FDA issues guidance on AI use in drug and biologicals regulatory decision making
Policies & Legislation
ANVISA and Danish Medicines Agency renew health regulatory collaboration
Colombia and Brazil introduce reforms to enhance healthcare regulation
Colombia boosts health sovereignty through public-private biotech collaboration agreement

Home/Pharma News Posted 07/04/2025
Bio-Thera partners with Tabuk in Saudi Arabia and SteinCares in LATAM

Home/Pharma News Posted 18/02/2025
Klinge-Teva and MS Pharma agreements for Eylea and Stelara biosimilars in Europe and MENA

Home/Pharma News Posted 06/02/2025
The best selling biotechnology drugs of 2008: the next biosimilars targets

Post your comment