ETHYL CORP. IBUPROFEN PLANT CAPACITY EXPANSION

ETHYL CORP. IBUPROFEN PLANT CAPACITY EXPANSION is planned at its Orangeburg, South Carolina site for completion by the end of the first quarter of 1991. Ethyl, the world's second largest manufacturer of bulk ibuprofen, currently has the capacity to produce over 2,300 metric tons of ibuprofen annually. The company did not disclose the specific change in capacity. Ethyl is basing its expansion plans on estimates that ibuprofen's share of the OTC analgesic market in the U.S. will grow from its current 18% to 30% in the 1990s. "The over-the-counter market for ibuprofen is expected to grow rapidly throughout the world and we want to be prepared for this increase in demand," James J. Compass, VP of Ethyl's Performance Products Division, stated. The U.S. demand for ibuprofen could reach 3,500-4000 metric tons in the early 90's, the firm believes. More than 20 companies have approval from FDA to market ibuprofen in the U.S., and all are customers of Ethyl, according to the company. Ethyl also announced Jan. 10 the availability of developmental quantities of an optically-active S(+) form of ibuprofen for evaluation and testing. Ethyl has been producing ibuprofen at its Orangeburg plant since 1977. North American demand for the compound has grown nearly 10-fold since then, according to the firm. The company also exports ibuprofen. Britain's Boots plc., which introduced ibuprofen in 1974, is still the largest bulk manufacturer of the compound in the world, although Boots' patent expired in 1986. Currently the company manufactures ibuprofen in a 3,000-ton-per-year facility in Nottingham, England. In April 1988, Boots announced a joint venture with Hoechst Celanese to build a 2,500 ton-capacity U.S. ibuprofen production line at an existing Hoescht Celanese manufacturing facility in Texas at a cost of approximately $35 mil. ("The Pink Sheet" April 25, 1988, T&G-10). The Boots/Hoechst U.S. facility also is on schedule for a 1991 opening. The plant will have the ability to expand its capacity to 3,500 metric tons annually to meet market demand. Boots expects the Texas production line to be in full operation in the last quarter of 1991, with product available in early 1992. Meanwhile, Ethyl also announced Jan. 10 that it will begin site studies for a future European ibuprofen facility. "If it proves feasible, the new European plant would be built to enhance our market share in the worldwide market," Ethyl's Compass said.

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Pink Sheet for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Archive

Ocaliva: Still No Clarity On Why EU Court Opposed Revocation Of Approval

 

Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.

Final Chance To Have Your Say: Take Our Reader Survey This Week

 
• By 

This is your final call to participate in the survey to better understand our subscribers’ content and delivery needs. The deadline is 20 September.

Shape Our Content: Take The Reader Survey

 
• By 

We are conducting a survey to better understand our subscribers’ content and delivery needs. If there are any changes you’d like to see in coverage topics, article format, or the method in which you access the Pink Sheet – or if you love it how it is – now is the time to have your voice heard.

Brazil Pilots Digital Drug Pack Inserts

 

A new pilot aims to take Brazil closer to ‘digital transformation.’

More from Pink Sheet

‘Prices Can Remain Contaminated Indefinitely’: Advanz Brushed Aside On UK Liothyronine Appeal

 
• By 

England’s Court of Appeal has upheld a Competition Appeal Tribunal’s 2023 finding that Advanz and its former owner Cinven abused their dominant position in the UK market for liothyronine tablets by charging prices that were many orders of magnitude higher than the benchmark for fair pricing.

New EU Filings

 

Linerixibat, GSK's treatment for cholestatic pruritus in patients with primary biliary cholangitis, is among the latest products that have been filed for review by the European Medicines Agency for potential EU marketing approval.

Podium Policy Returns To US FDA, Or Is It Podcast Policy?

 

US FDA critics have long decried the practice of using informal communications to convey regulatory expectations as podium policy. In the Makary era, the phrase may need to be updated because the agency now seems to be specializing in policy by podcast.