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 Fluoxetine Tabs 60 mg approval solidifies the Company's position in the molecule by complementing the recent approval in April 2024 for Fluoxetine 10 mg and 20 mg tablets and Fluoxetine capsules Strides Pharma Science Limited (Strides) today announced that its step-down wholly owned subsidiary, Strides Pharma

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 Sun Pharma (Reuters: SUN.BO, Bloomberg: SUNP IN, NSE: SUNPHARMA, BSE: 524715, Sun Pharmaceutical Industries Limited, and includes its subsidiaries or associate companies) and Israel-based Moebius Medical Limited announced that the U.S. Food and Drug Administration (FDA) has granted Fast Track designation (FTD) to MM-II (Large

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  Zydus Lifesciences Limited (including its subsidiaries/ affiliates, hereafter referred to as “Zydus”) has received final approval from the United States Food and Drug Administration (USFDA) to market Scopolamine Transdermal System 1 mg/3 days. (USRLD: Transderm Scop Transdermal System ® 1 mg/3 days). This is the

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Lupin Limited announced on Thursday the launch of its generic cancer treatment drug in the US market. The Mumbai-based pharmaceutical firm has introduced Doxorubicin Hydrochloride Liposome Injection in single-dose vials. This launch follows the approval from the US Food and Drug Administration (FDA) received by Lupin’s

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ORSL® (औरसल), India’s #1 Electrolyte Drink, announced the launch of its new product line, Advanz Care. This innovative range offers three specialized variants designed to cater to a consumer’s diverse hydration, energy and immunity needs. As part of the portfolio of Advanz Care, ORSL® has launched

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Gland Pharma Limited (Gland or Company), a generic injectable-focused pharmaceutical company, has received tentative approval from the United States Food and Drug Administration (USFDA) for Latanoprostene Bunod Ophthalmic Solution, 0.024%. The Product is bioequivalent and therapeutically equivalent to the reference listed drug (RLD), Vyzulta® Ophthalmic Solution,

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The U.S. Centers for Disease Control and Prevention has recommended that individuals aged six months and older should be given an updated COVID-19 vaccine for the 2024-25 immunization campaign, irrespective of whether they have previously been vaccinated for the disease. The agency's recommendation on Thursday echoed

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Wanbury Ltd, one of India’s fast growing pharmaceutical company having a presence in API global market and domestic branded formulation today announced the successful completion of the United States Food & Drug Administration (USFDA) inspection at Patalganga site, Maharashtra. The inspection that started from Monday,

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Rising inactivity, increased screen time, & popularized junk food consumption in children have heavily contributed to this Hypertension or high blood pressure (BP) has recently become increasingly prevalent among children and young adults. Causes of pediatric hypertension including overweight and obesity, heart defects, kidney problems, poor

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