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About 1351 results for "food and drugs administration"

Severe, Persistent Joint Pain Warning Issued for Diabetes Drug Class
Monthly Prescribing Reference

Severe, Persistent Joint Pain Warning Issued for Diabetes Drug...

Share this article: The Food and Drug Administration (FDA) is warning that use of dipeptidyl peptidase-4 (DPP-4) inhibitors may cause joint pain which may be severe and disabling. DPP-4 inhibitors are a class of drugs used as adjunct to diet and ... Monthly Prescribing Reference, 1 hour ago

648 images for food and drugs administration

Irish Times, 5 days ago
EthioScoop, 6 hours ago
News 9, 1 week ago
Providence Business News, 3 days ago
Savannah Morning News, 1 week ago, 3 days ago
Reuters UK, 3 days ago
Business Insider, 3 days ago, 3 days ago
FOX 5 KVVU-TV, 1 week ago
Money Control

Sun, Wockhardt recall drugs from US market

According to a notification issued by the US Food and Drug Administration, Sun Pharma's recall was initiated last month under Class-III classification which was as 'a situation in which use of or exposure to a violative product is not likely to cause adverse ...
 Money Control21 hours ago Sun Pharma, Wockhardt recall drugs from US market  Business Today India1 day ago 2 Indian-Based Pharmaceuticals Recall Their Drugs From The US Market  MedIndia2 hours ago Wockhardt recalls over 1.62 lakh cartons of drugs in US  Economic Times1 month ago
Times of India

Will female Viagra liberate Indian women?

The first prescription drug to enhance women's sexual drive won regulatory approval from the Food and Drug Administration recently, clinching a victory for a lobbying campaign that had accused the FDA of gender bias for ignoring the sexual needs of ...
 Times of India5 days ago Expert warns over Pink Viagra dangers  Trade Arabia6 days ago Female 'viagra' drug: Did cynical marketing override medical science?  WA Today1 week ago 'Female Viagra' approved by US drugs agency  MSN News US1 week ago

Indian Pharma Gets USFDA Approval To Market Tablets To Treat Osteoporosis In The US

The US Food and Drug Administration (USFDA) has approved Indian drug firm, Aurobindo Pharma, to manufacture and market its generic version of Eli Lilly's Evista tablets used to treat and prevent osteoporosis in postmenopausal women. The approval ...
 MedIndia3 hours ago Aurobindo Pharma Ltd bounced off its 50-day moving average today. Know why  Business Insider India4 days ago Aurobindo Pharma gets USFDA nod for osteoporosis drug  The Hindu1 day ago Lupin gains in volatile trade after reports of receiving USFDA approval for a drug  Business Standard5 days ago
CBS News

Will FDA food labels change the way you eat?

The U.S. Food and Drug Administration is expected to roll out updated nutrition labels on food packages next year in the hopes of making them more realistic and useful. The agency plans to revise serving sizes to better reflect the amount of food ...
 CBS News4 days ago Edurant Label Updated With New Pediatric Indication, Warning  Monthly Prescribing Reference3 days ago US Regulators Urge To Include More Detail About Added Sugars on Food Labels  Med India1 month ago FDA proposes putting percent daily value of added sugar on food labels  Reuters1 month ago
Times of India

FDA seizes substandard betel nut, black pepper valued at Rs 17.76 lakh in Nagpur

A team of Food and Drug Administration (FDA) officials conducted a raid at a godown of Verma Roadways at Waddhamana on Amravati road and seized substandard betel nut and black pepper.
 Times of India3 days ago After complaints, FDA collects samples from Amul godown  Economic Times1 month ago After plaints, samples taken from Amul godown  Times of India1 month ago
Global Research

The Insidious Relationship between The U.S. Food and Drug Administration (FDA) and Big Pharma

The Food and Drug Administration (FDA) is aiding and abetting criminal companies. There are various solutions to this ongoing catastrophe that would depend on the basic honesty of Big Pharma. That honesty doesn't exist. And the Dept. of Justice ...
 Global Research5 days ago FDA approves Sun Pharma's inflammatory drug  Bio Spectrum Asia1 week ago UP Food safety officials raid Vishal Mega Mart, seize products  Economic Times1 month ago Carcinogens, banned dye found in mid-day meal  Times of India1 month ago
Med India

Goa FDA Officials Collect Four More Noodle Samples for Lab Testing

The Goa Food and Drugs Administration (FDA) has collected four more samples of packed instant noodles for testing, revealed an official statement. In all, more than a dozen noodle brands are under FDA's scanner, ever since the controversy surrounding the lead ...
 Med India2 months ago Maggi ban: Regulator overreach, says Nestle counsel  Rediff.com1 month ago Maggi issue: Will food regulator move the Supreme Court?  Rediff.com1 week ago US food regulator testing Maggi noodles after India recall  Rediff.com2 months ago

Gujarat shares Maggi sample testing method with USFDA

India | Ahmedabad June 23, 2015 Last Updated at 16:22 IST The Gujarat Food and Drugs Control Administration has shared the methods and protocols of food sample testing adopted in the case of Nestle's famous noodle brand Maggi with the US Food and Drug ...
 Business Standard2 months ago Sunfeast Yippee ban: ITC says not consulted, Gujarat FDCA contests view  Rediff.com1 month ago Gujarat bans Yippee noodles, Bambino Macaroni after tests reveal MSG, lead content  First Post.com1 month ago After Maggi, Yippee noodles and Bambino Macaroni banned in Guj  One India1 month ago

Maggi case: Nestle violated laws, alleges Maharashtra FDA

The Food and Drugs Administration of Maharashtra today told the Bombay High Court that Maggi noodles manufacturer Nestle India violated laws with the lead level in the popular instant snack being above the permissible limit. The court was hearing a ...
 Business Standard1 month ago Nestle violated laws with excess lead in Maggi, Maha FDA tells Bombay High Court  First Post.com1 month ago Nestle violated laws: FDA to Bombay High Court  Asian Age1 month ago Maggi row: Maharashtra FDA says Nestle violated laws  Asian Age1 month ago
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