Unilever has sued Hampton Creek, a start-up food company that is developing animal-free alternatives to industrialised foods over the definition of mayonnaise. The lawsuit was filed in Newark, NJ, in a federal court on October 31, ...
Tags: mayonnaise, false advertising, Agriculture
Ross Hydropneumatic Tanks and Pressure Vessels are built in any capacity up to 100,000 gallons, with working pressures from 50 to 200 psig, for indoor or outdoor installation. Available in carbon steel, 316 and 304 stainless steel, Monel, ...
Tags: Ross Hydropneumatic Tanks, Pressure Vessels, Decoration
Ross Engineering is a custom manufacturer of ASME pressure vessels as well as storage tanks, stirred reactors, sanitary vessels and columns. With decades of experience in design and fabrication, the company has grown to be one of the ...
Tags: ASME Pressure, Ross Engineering
Cubist Pharmaceuticals has entered into two separate agreements to acquire Optimer Pharmaceuticals and Trius Therapeutics, as part of the company's Building Blocks of Growth strategy to strengthen its presence in acute care and hospital ...
Dr Reddy's Laboratories, an India-based pharmaceutical company, has introduced Donepezil Hydrochloride tablets 23mg in the US on 26 July 2013. The launch follows the approval of an abbreviated new drug application (ANDA) for the drug by ...
Tags: Drug Aricept, Generic Equivalent
American Regent, a subsidiary of a Daiichi Sankyo Group Company named Luitpold Pharmaceuticals, has won USFDA approval for Injectafer (ferric carboxymaltose injection) for the treatment of iron deficiency anemia (IDA). A parenteral iron ...
Tags: Iron Deficiency Anemia, Medicine
Ross Engineering Inc., a custom fabricator of storage tanks, pressure vessels and reactors, has acquired new machining equipment and upgraded its facility to better serve customers. It can now take fabrication projects of virtually any size ...
Tags: Construction, Decoration
The USFDA has cleared Actavis' abbreviated new drug application (ANDA) for Lamotrigine orally disintegrating tablets, 25mg, 50mg, 100mg and 200mg. A generic version of GlaxoSmithKline's Lamictal ODT, the antiepileptic drug is indicated ...
The USFDA has accepted Pfizer's supplemental new drug application (sNDA) to expand labeling of rheumatoid arthritis medication Xeljanz (tofacitinib citrate) to include inhibition of structural damage progression. The data from ORAL Start ...
Tags: FDA, Pfizer sNDA, Xeljanz Labeling
Abyrx, a US-based therapeutic device company, has received the US Food and Drug Administration (FDA) approval for its new Absorbable Hemostatic Bone Putty (AHBP) for clinical use. AHBP is a surgical ready-to-use product which achieves ...
Tags: Abyrx, Bone Putty
Specialty pharmaceutical company Sun Pharmaceutical Industries has obtained final USFDA approval for the abbreviated new drug application of generic Depo-Testosterone Injection, Testosterone Cypionate Injection USP, 100mg/ml and 200mg/ml. ...
The USFDA has granted priority review designation for investigational agent Metreleptin, jointly developed by Bristol-Myers Squibb Company and AstraZeneca, for the treatment of metabolic disorders associated with rare forms of ...
A desiccant is a material that removes moisture from the air and is a hygroscopic substance that induces or sustains a state of dryness in its local vicinity in a moderately well-sealed container. This material for specialized purposes may ...
The USFDA has accepted Teva Pharmaceutical Industries' supplemental new drug application (sNDA) for reviewing Copaxone (glatiramer acetate injection) 40mg/1mL. Indicated for patients with relapsing-remitting multiple sclerosis (RRMS), the ...
Tags: Drug Application, Medicine
The USFDA has approved Novartis' Ilaris (canakinumab) for the treatment of active systemic juvenile idiopathic arthritis (SJIA) in patients with two years age and more. The first interleukin-1 beta inhibitor is the only treatment approved ...