Search For "usf"
US FDA inspection closed at its Injectable Facility with Zero 483 observat
Updated : 1 year, 11 months ago IST
According to the stock market filing with the National Stock Exchange, the U.S. FDA carried out the inspection between June 10 to June 13, 2024, and concluded with zero 483 observations. The pharma major said in its filing, "The United States Food and Drug Administration (U.S. FDA) has compl
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Cipla secures USFDA approval for pancreatic disease injection, shares surg
Updated : 2 years ago IST
Mumbai-headquartered pharma major, Cipla's US arm has secured final approval from the United States Food and Drug Administration (USFDA) for its Lanreotide Injection 120 mg/0.5 mL, 90 mg/0.3 mL, and 60 mg/0.2 mL.
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Utkarsh Small Finance Bank Leads the Way with Interoperable Cardless Cash
Updated : 2 years, 8 months ago IST
Mumbai (Maharashtra) [India], September 22: Utkarsh Small Finance Bank Limited (“USFBL” or the “Bank”), today announced the launch of an innovative service, set to revolutionise cash withdrawal experiences. Utkarsh Small Finance Bank is dedicated to offering process-centric, technology-drive
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Ujjivan Small Finance in partnership with BUSINESSNEXT wins the Best CRM I
Updated : 2 years, 11 months ago IST
Mumbai (Maharashtra) [India], June 20: Ujjivan Small Finance Bank (USFB) Limited, one of the leading small finance banks catering to the un-served and under-served segments, won the 'Best CRM implementation' award. The CRM initiative, in collaboration with BUSINESSNEXT, a universe of composa
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Aaquaries Global Industries Limited conferred with the prestigious "Innova
Updated : 3 years, 1 month 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 : 3 years, 1 month 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 : 3 years, 1 month 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, 2 months 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, 2 months 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, 4 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, 5 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, 5 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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