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FDA announces approval of vaccines for 2010-2011 US influenza season

The U.S. Food and Drug Administration announced today that it has approved vaccines for the 2010-2011 influenza season in the United States. Seasonal influenza vaccine protects against three strains of influenza, including the 2009 H1N1 influenza virus, which caused the 2009 ...

Cognis exclusively licensed two new active ingredients from IMD

Specialty chemicals supplier Cognis and InterMed Discovery (IMD), a world class natural product lead-discovery company, are continuing their strategic cooperation: Cognis has now exclusively licensed two new active ingredients for weight management and cognitive performance from ...

Brand-Nu Laboratories adds Chlophedianol Hydrochloride to API line

Brand-Nu Laboratories, a leading US-based high purity chemical manufacturer and distributor, has introduced Chlophedianol Hydrochloride, also known as Clofedanol Hydrochloride JP, to its product portfolio of active pharmaceutical ingredients (APIs). With the controversy ...

B. Braun Medical announces availability of large volume heparin infusion solutions

B. Braun Medical Inc. (B. Braun) announced today the availability of large volume heparin infusion solutions. Based on the new United States Pharmacopeia (USP) standards for heparin products released by the U.S. Food and Drug Administration (FDA) in October 2009, changes to B. ...

FDA opens two-day hearing to examine safety of diabetes drug Avandia

The Fiscal Times: "There will be more at stake than just one drug's future when the Food and Drug Administration opens a two-day hearing Tuesday on the safety of the diabetes drug Avandia. The 30-member panel of outside experts will also be rendering judgment on research methods ...

Access announces agreement to develop oral formulation of proprietary injectable drugs

Access Pharmaceuticals, Inc. (OTC Bulletin Board: ACCP),announced today that it has entered into a pre-licensing feasibility agreement with a leading biotechnology company to develop an oral formulation of its currently-marketed, proprietary injectable drugs. Access will utilize ...

OraVerse MAA accepted for review in five key European countries

Sanofi-Aventis Deutschland GmbH and Novalar Pharmaceuticals, Inc. today announced that the Marketing Authorization Application (MAA) for OraVerse has been accepted for review by the regulatory agencies of the United Kingdom (UK), Germany, Italy, France and Spain. OraVerse is the ...

BASF increases prices for beta-carotene and its derivates

Ludwigshafen , Germany July 14, 2010 BASF globally increases the prices for beta-carotene and its derivatives canthaxanthin and apocarotenal by 12% with immediate effect or as existing commitments allow. The price increase includes all products for human and animal nutrition. All ...

2010 H1 report: Jiangsu Kanion Pharmaceutical (600557.SH)

BEIJING, Jul 25, 2010 (Xinhua via COMTEX) -- The following is a table showing the main business indicators for the first half of 2010 of Shanghai-listed Jiangsu Kanion Pharmaceutical Co. Ltd. (600557.SH): First half of 2010 First half of 2009 Earnings per share (yuan) 0.29 0.22 ...

Eli Lilly completes Alnara acquisition

Eli Lilly and Company (NYSE: LLY) today announced that it has completed the acquisition of Alnara Pharmaceuticals, Inc., a privately-held company developing protein therapeutics for the treatment of metabolic diseases. The transaction, first announced on July 2, 2010, has ...

FDA approves Mylan's ANDA for generic Catapres-TTS

Mylan Inc. (Nasdaq: MYL) today announced that its subsidiary Mylan Technologies Inc. has received final approval from the U.S. Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA) for Clonidine Transdermal System USP, 0.1 mg/day, 0.2 mg/day and 0.3 ...

First generic version of Lovenox receives FDA approval for DVT

The U.S. Food and Drug Administration today approved the first generic version of Lovenox (enoxaparin sodium injection), an anti-coagulant drug used to prevent deep vein thrombosis (DVT), a potentially deadly blood clotting condition. Approved for use in 1993, Lovenox is made ...

FDA Advisory Committee recommends approval of AstraZeneca's ticagrelor for Acute Coronary Syndromes

AstraZeneca (NYSE: AZN) today announced that theUS Food and Drug Administration (FDA) Cardiovascular and Renal Drugs AdvisoryCommittee recommended the FDA approve AstraZeneca's investigational drug ticagrelor for the reduction of thrombotic events in patients with Acute Coronary ...

FDA accepts for filing Cladribine Tablets NDA for MS

EMD Serono, Inc., an affiliate of Merck KGaA, Darmstadt, Germany, announced today that the U.S. Food and Drug Administration (FDA) has accepted for filing the New Drug Application (NDA) for Cladribine Tablets as a therapy for relapsing forms of multiple sclerosis (MS). The ...

China Sky One Medical receives SFDA approval for producing Ciclopirox Olamine Vaginal Suppositories

China Sky One Medical, Inc. ("China Sky One Medical" or "the Company") (Nasdaq: CSKI), a leading fully integrated pharmaceutical company in the People's Republic of China ("PRC"), today announced that the Company has obtained approval from the State Food and Drug Administration ...

Xeomin receives FDA approval for treatment of cervical dystonia

Merz Pharmaceuticals today announced that the United States (U.S.) Food and Drug Administration (FDA) has approved Xeomin (incobotulinumtoxinA), a botulinum toxin type A for the treatment of adults with cervical dystonia or blepharospasm. According to an epidemiology study ...

Victory Pharma acquires assets of MiddleBrook Pharmaceuticals

Victory Pharma, Inc. ("Victory") today announced that it has completed the acquisition of substantially all of the assets of MiddleBrook Pharmaceuticals, Inc. (OTCQB: MBRKQ). Through the acquisition, Victory Pharma has expanded its product portfolio with the addition of anti...

BASF declares Force Majeure on Plastomoll DNA, Palatinol N, Hexamoll DINCH and selected Palamoll grades

Ludwigshafen , Germany July 21, 2010 Due to a shortage of raw materials caused by an unforeseeable technical defect in its iso-Nonanol (INA) plant in Ludwigshafen, Germany, BASF SEis currently unable to produce the plasticizers Plastomoll DNA, Palatinol N, Hexamoll DINCH and ...

BASF raises prices for isophorone diamine in Europe

BASF is raising its prices for isophorone diamine (IPDA) in Europe by 200 per metric ton, or by the corresponding amount in local currency, effective immediately or as existing contracts permit. The IPDA specialty amine is valued as a curing agent for epoxy resins and as an ...

Weifang Shengtai to supply Kelun with 10,000 tons of dextrose monohydrate injection grade

Shengtai Pharmaceutical, Inc. (OTC Bulletin Board: SGTI) announced on August 6, 2010 that Weifang Shengtai Pharmaceutical Co., Ltd ("Weifang Shengtai"), its operating subsidiary in China, entered into an agreement with Kelun Pharmaceutical ("Kelun") to supply Kelun with 10 ...
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