Kwality Pharmaceuticals receives approval for Tamoxifen 20mg Tablet in South Africa
This approval is a significant achievement in expanding the availability of this critical therapeutic,
This approval is a significant achievement in expanding the availability of this critical therapeutic,
The transaction is expected to result in approximately $175 million to support further development of IMG-007
Divalproex Sodium Delayed-Release Capsules USP, 125 mg have an estimated market size of US$ 61.1 million for twelve months ending September 2024 according to IQVIA
FDC Ltd has received final approval from USFDA for the company's Abbreviated New Drug Application (ANDA) for Cefixime 400 mg Tablets
The TGA approval marks a pivotal step in Rusan Pharma’s expansion into the Australian market
Till 30th November 2024, more than 2690 PACS have been given initial approval and 687 Kendras have been opened in PACS
This product is indicated in coagulation disorders caused by vitamin K deficiency or interference with vitamin K activity.
The successful completion of RRA assessment by the USFDA, would enable company to open up its business in the USA market
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