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Rizatriptan aurobindo mirtazapin aurobindo 15 mg

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Kindly visit the Manage my subscription page to discover the benefits of this programme. According to IMS data, the annual sales of Rizatriptan Benzoate Tablets were approximately $300 million in the United States for the twelve months ended March 2012. If you think you may have a medical emergency, please call your doctor or 911 immediately. NCD Codes that may be related to Rizatriptan Benzoate with NDC 65862-599 is a a human prescription drug product labeled by Aurobindo Pharma Limited. The product has been approved out of Unit VII (SEZ) formulations facility at Hyderabad, Aurobindo said. The company made the announcement during trading hours today, 1 January 2013. If you have questions or concerns about the substances you are taking, check with your healthcare provider. The company's robust product portfolio is spread over 6 major therapeutic/product areas encompassing Antibiotics, Anti-Retrovirals, CVS, CNS, Gastroenterologicals, and Anti-Allergics. The stock had hit a 52-week low of Rs 85.05 on 2 January 2012. The stock had outperformed the market over the past one month till 31 December 2012, rising 0.66% compared with the Sensex's 0.45% rise. The information in this website is intended for healthcare providers and consumers in the United States. The mid-cap pharmaceutical company has equity capital of Rs 29.11 crore. Welcome to the premium services of Business Standard brought to you courtesy FIS. Copyrights © 2018 Business Standard Private Ltd. The stock hit a high of Rs 193.90 and a low of Rs 190.40 so far during the day. Non-Proprietary Name Rizatriptan Benzoate. The absence of a warning or notice for a given drug or drug combination is not indication that the drug or drug combination are safe, appropriate or effective for any given patient. Cookie Policy unless you have disabled them. On BSE, fenistil gel verbrennung 1 lakh shares were traded in the counter as against average daily volume of 3.54 lakh shares in the past one quarter. All contents of this website are provided on an "as is" and "as available" basis without warranty of any kind. Aurobindo Pharma has received final approval from the United States Food and Drug Administration (USFDA) to manufacture and market Rizatriptan Benzoate Tablets 5mg (base) and 10mg (base), which was earlier tentatively approved. Drug maker Aurobindo Pharma Ltd on Tuesday said it has received final approval from the US Food and Drug Administration (USFDA) to manufacture and market Rizatriptan Benzoate Tablets used in the treatment of migraine. Rizatriptan Benzoate Tablets 5mg (base) and 10mg (base) is the generic equivalent of Merck and Co's Maxalt Tablets of equivalent dose and is indicated for the acute treatment of migraine with or without aura in adults and in pediatric patients 6 to 17 years old. You can change your Cookie Settings at any time but parts of our site will not function correctly without them. Aurobindo Pharma, headquartered at Hyderabad in Andhra Pradesh, manufactures generic pharmaceuticals and active pharmaceutical ingredients (APIs).

Gabapentin aurobindo

The contents of the National Drug Codes List website are provided for educational purposes only and are not intended in any way as medical advice, medical diagnosis or treatment. Aurobindo now has a total of 171 abbreviated new drug application (ANDA) approvals (146 Final approvals including 2 from Aurolife Pharma LLC and 25 Tentative approvals) from USFDA, according to Aurobindo. The scrip had also outperformed the market in past one quarter, verformte fingernägel jumping 33.59% as against Sensex's 3.54% gain. The product is ready for launch, Aurobindo said in a statement. Aurobindo Pharma reported consolidated net profit of Rs 222.35 crore in Q2 September 2012, compared with net loss of Rs 80.16 crore in Q2 September 2011. Rizatriptan Benzoate Tablets 5mg (base) and 10mg (base) is the generic equivalent of Merck and Co's Maxalt Tablets 5mg (base) and 10mg (base) and is indicated for the acute treatment of migraine with or without aura in adults and in pediatric patients 6 to 17 years old. The product has been approved out of Unit VII (SEZ) formulations facility in Hyderabad. The company is marketing these products globally, in over 125 countries. Reliance on any information provided by the National Drug Codes List website or other visitors to this website is solely at your own risk. The annual sale of the product is approximately $300 million for 12 months ending March 2012 according to IMS data, feenflügel groß the release said. Aurobindo scrip is traded at Rs 193.25 apiece on BSE in the afternoon trade. The product which was tentatively approved by the FDA earlier, is ready for launch, methotrexat morbus crohn a statement from Aurobindo said. Many of Over the Counter drugs are not reviewed by the FDA but they might be marketed to the public if the product complies with the applicable rules and regulations. Meanwhile, the BSE Sensex was up 160.02 points or 0.82% at 19,586.73. The stock had hit a 52-week high of Rs 201.40 on 5 December 2012. Aurobindo now has a total of 171 abbreviated new drug application (ANDA) approvals (146 final approvals including 2 from Aurolife Pharma LLC and 25 tentative approvals) from USFDA. The company's manufacturing facilities are approved by several leading regulatory agencies like US FDA, UK MHRA, gel batterie für boote WHO, Health Canada, MCC South Africa, ANVISA Brazil. Net sales rose 40.9% to Rs 1481.05 crore in Q2 September 2012 over Q2 September 2011.

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