Search For "usfda"
Aaquaries Global Industries Limited conferred with the prestigious "Innova
Updated : 2 years, 10 months ago IST
New Delhi [India], April 19 (ANI/SRV): Aaquaries Global Industries Limited, Mumbai based top research-driven pharmaceutical company started in the year 2007 focusing on contract manufacturing APIs from Natural Extracts for Malaria Anti - Cancer & various other segments & a leading ex
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Zydus receives final approval from US regulator for Azithromycin tablets
Updated : 2 years, 11 months ago IST
Azithromycin is prescribed to treat certain bacterial infections such as bronchitis, pneumonia, sexually transmitted diseases (STD), and infections of the ears, lungs, sinuses, skin, throat, and reproductive organs.
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Samples of eye drops linked to blindness, deaths in US are "free of contam
Updated : 2 years, 11 months ago IST
The samples of eye-drops manufactured by India's Global Pharma Healthcare,which were linked to three deaths and blindness in some patients in US, are found to be "free of contamination", said Health Ministry sources on Tuesday.
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USFDA inspection at Karakhadi unit completed without any observations: Ale
Updated : 3 years ago IST
According to a company statement released on Monday, the inspection was done between March 6 and March 10 this year.
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makeO (formerly toothsi) appoints Japan Doshi as its Chief Product and Tec
Updated : 3 years ago IST
New Delhi [India], March 1 (ANI/PNN): makeO, India's first and only USFDA-approved D2C aligner company, is thrilled to introduce Japan Doshi as its new Chief Product and Technology Officer (CPTO). Japan's experience in the tech industry spans over a decade with senior roles at e-commerce gia
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UAE-based Niner Pharmaceuticals LLC Aims to Develop an End-to-end Supply C
Updated : 3 years, 2 months ago IST
New Delhi [India], January 4 (ANI/PNN): Niner Pharmaceuticals LLC, a UAE-based pharmaceutical company, plans to develop an end-to-end supply chain between the Indian market and the GCC markets. With this aim, the company is investing in the Indian market by assembling world-class manufacturi
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Alembic Pharma gets US regulator final nod for skin ointment - Desonide Cr
Updated : 3 years, 3 months ago IST
According to a statement from the Vadodara-headquartered pharma firm, the ANDA was filed by Aleor Dermaceuticals (Aleor) which was amalgamated with Alembic. The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD), Desonide Cream, 0.05 per cent, of Padagis U
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USFDA lists Sun Pharma's Halol unit under 'import alert'
Updated : 3 years, 3 months ago IST
According to a statement from the pharmaceutical company to the stock exchanges, the Import Alert implies that all future shipments of products manufactured at this facility are subject to refusal of admission to the US market until the facility becomes compliant with CGMP standards.
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Zydus gets USFDA's final nod to market antifungal Micafungin for injection
Updated : 3 years, 4 months ago IST
Zydus Lifesciences has received approval from US Food and Drug Administration to market Micafungin.
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Concept Medical Inc. and its subsidiary Envision Scientific marked their F
Updated : 3 years, 4 months ago IST
Surat (Gujarat) [India], October 20 (ANI/PNN): Concept Medical Inc and its group company Envision Scientific, the world's leading medical device manufacturing company, celebrated their Founder's Day and Azadi Ka Amrit Mahotsav on Tuesday with the 'Mega Voluntary Blood Donation Camp' at all t
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Magnum receives USFDA 510k clearance for its surgical masks
Updated : 3 years, 6 months ago IST
New Delhi [India], August 26 (ANI/SRV): Magnum, one of the largest mask manufacturers from Mumbai, which has been in this industry for the last 29 years has recently received the US Food and Drug Administration (FDA) 510 (k) clearance, which is an approval by the United States government tha
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Zydus receives final approval from USFDA to market Colestipol Hydrochlorid
Updated : 4 years ago IST
Ahmedabad (Gujarat) [India], March 15 (ANI): Zydus Lifesciences Ltd. has received final approval from the United States Food and Drug Administration (USFDA) to market Colestipol Hydrochloride Tablets in the strength of 1mg (US RLD: Colestid), said the pharmaceutical company on Monday.
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