The US arm of Aurobindo Pharma is recalling 47,040 bottles of Venlafaxine Hydrochloride extended release capsules, manufactured by the... ...http://www.business-standard.com/article/pti-stories/aurobindo-recalls-47k-bottles-of-antidepressant-capsules-in-us-117022200963_1.html
In 2011, the U.S. Food and Drug Administration approved digital breast tomosynthesis (DBT) for use with full-field digital mammography (FFDM) in... ...http://feedproxy.google.com/~r/allhealthnews/~3/FuQbqryD0Lc/breast-tomosynthesis-technique-reduces-screening-recall-rate-168012-1.htm
(Reuters) - Amphastar Pharmaceuticals Inc said on Tuesday that the U.S. Food and Drug Administration had rejected its application to market an... ...http://feeds.reuters.com/~r/reuters/INhealth/~3/UD3uKaTA83k/us-amphastar-pharms-fda-idINKBN16018Y
Haryana Food and Drugs Administration teams today raided seven private hospitals in various cities to ensure no hospital violates the Centre's... ...http://www.dnaindia.com/health/report-7-hospitals-raided-to-check-stents-price-in-haryana-2329378
The Haryana Food and Drugs Administration (FDA) on Monday raided leading private hospitals at Panchkula, Sonipat and Gurugram where cardiac stent... ...http://www.prokerala.com/news/articles/a720204.html
An additional reason precisely why...