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BENGALURU (Reuters) -Indian drugmaker Cipla said on Friday its U.S. unit was recalling six batches of albuterol sulfate inhalation aerosol due to a "container defect". "The company is initiating a ...
The company's share price has fallen nearly 20% since Friday when it first issued a voluntary recall of its own supplements. On Wednesday, they closed down 3.8% at 4,875 yen.
Kobayashi Pharmaceutical did not have GMP certification, and had no opportunity to have a third party check it. Under the guidelines for voluntary recalls, Kobayashi Pharmaceutical had a policy of not recalling products until a causal relationship could be established to some extent, possibly resulting in further widespread health issues. [3]
People have had to have their eyes surgically removed due to the bacteria
This contamination was not detected until 2018. The incident, according to medicinal chemist and pharmaceutical industry blogger Dr. Derek Lowe, points to a greater problem. Generic drug manufacturers often change the way in which prescription drug ingredients are made in order to lower costs of making them, so this kind of contamination may be ...
A drug recall removes a prescription or over-the-counter drug from the market. Drug recalls in the United States are made by the FDA or the creators of the drug when certain criteria are met. When a drug recall is made, the drug is removed from the market and potential legal action can be taken depending on the severity of the drug recall.
Essential is an Indian pharmaceutical manufacturing company that constructs active pharmaceutical ingredients as well as intermediary products. The 40-acre facility unit was constructed on the Andhra Pradesh Industrial Infrastructure Corporation campus with a ₹200 crore budget and began production in April 2019. [1]
The latest recalls and warnings underscore the need to properly vet your eye drops and other eye care products, say experts.