usfda การใช้

• The vaccine is pending approval by the USFDA.
• Today, the USFDA-approved fruit processing plant is one of the largest in Asia.
• In April 2011 a second generic formulation, from Wockhardt, received tentative USFDA marketing approval.
• After determining the risks outweigh the benefits, the USFDA requested physicians stop prescribing the drug.
• The USFDA granted generally recognized as safe ( GRAS ) status for high alpha linolenic flaxseed oil.
• This product, called CorLiCyte, will be used in a USFDA trial to heal diabetic wounds.
• Rolapitant has a significantly long half life of 160 hours and got approval by the USFDA in 2015.
• Abatacept in a subcutaneous administration form has been approved by USFDA, for self-administration by the patient.
• The first generic donepezil became available in November 2010 with the USFDA approval of a formulation prepared by Ranbaxy Labs.
• The USFDA granted market clearance to the Caya?contoured diaphragm in late 2014, and Kessel is seeking a partner for US market introduction.
• Sun Pharma requested the USFDA to withdraw approval for 28 Abbreviated New Drug Applications ( ANDAs ) belonging to its wholly owned subsidiary Ranbaxy Laboratories.
• In 2010, he became co-director of the Environmental Bioinformatics and Computational Toxicology Center, a Rutgers-Princeton-USFDA Research Consortium.
• State-of-the-art manufacturing units at Paonta Sahib ( Himachal Pradesh ), built as per the USFDA / WHO guidelines.
• Three years later in 1999, the company received USFDA approval for Aciphex ( rabeprazole ), a drug co-marketed with Johnson & Johnson.
• That is what has enabled one of its manufacturing facility to get approved by leading pharmaceutical stringent regulatory authorities such as the USFDA and World Health Organisation.
• While Russia, Poland, and Ukraine have approved this procedure, the United States Food and Drug Administration ( USFDA ) has not yet granted its approval.
• The USFDA has conferred orphan drug status on Pluristem's PLX cells for the treatment of Buerger's disease ( 2011 ) and aplastic anemia ( 2013 ).
• The manufacturing facility at Dholka and the API unit at Ankleshwar in Gujarat are USFDA-certified; the overseas manufacturing facility at Ethiopia is the WHO-cGMP compliant facility.
• He gained a good experience working at R & Ds of top 10 companies of Indian Pharma . and is currently leading a program pursuing complex parenteral projects for USFDA approvals.
• But he maintained that it was " important to have an agreed set of principles so we can use money to buy drugs that the USFDA has not approved ."