Healthcare
Large-cap - With a market cap of ₹4059.91 Cr.
EX-Date | Purpose |
---|---|
27 05 2021 | Final Dividend & Audited Results |
30 07 2021 | Quarterly Results |
02 11 2021 | Quarterly Results |
31 01 2022 | Interim Dividend |
30 05 2022 | Final Dividend & Audited Results |
29 07 2022 | Quarterly Results |
01 11 2022 | Quarterly Results |
31 01 2023 | Quarterly Results & Interim Dividend |
26 05 2023 | Final Dividend & Audited Results |
03 08 2023 | Quarterly Results |
01 11 2023 | Quarterly Results |
31 01 2024 | Interim Dividend & Quarterly Results |
28 10 2024 | Quarterly Results |
31 01 2025 | Quarterly Results & Interim Dividend |
22 05 2025 | Final Dividend & Audited Results |
31 07 2025 | Quarterly Results |
The said transaction is expected to be completed by January 31, 2025
Total consolidated income of the company increased by 12.07% to Rs 11037.50 crore for Q2FY23
Total consolidated income of the company increased by 13.12% at Rs 12486.02 crore for Q2FY24
The two partner companies will share post-commercialization economics in about 45(Philogen):55(Sun Pharma) ratio
Total consolidated income of the company increased by 12.83% at Rs 12145.28 crore for Q1FY24
The objective of acquisition is to facilitate consolidation of business in Israel
The company is recalling the affected lot, produced at its Mohali plant, due to ‘discoloration’
The agreement includes an upfront payment of $15 million, regulatory and commercial milestones, and royalties
Taro Pharma Corporation is set up as an entity separate from Alchemee LLC, a subsidiary of Taro Israel, to help Alchemee LLC with selling its Proactiv skincare products on e-commerce marketplace in USA
Besides, the company has executed an additional agreement to acquire further around 4.04% equity shares in Agatsa Software
The company has obtained rights from Daewoong Pharmaceutical Co, Korea to manufacture and commercialise FEXUCLUE (Fexuprazan) in India
The USFDA has excluded 14 products from this Import Alert subject to certain conditions
This acquisition is an opportunity to bring deuruxolitinib to market globally and make a meaningful difference to alopecia areata patients around the world
The company is recalling 24,194 prefilled syringes of Fyremadel (ganirelix acetate) injection
Currently, there are no phenobarbital injection products approved by the US FDA for the treatment of seizures in newborns
The plant was inspected in August and had received a form 483 with six observations earlier
Sun Pharmaceutical Industries Inc is recalling the product for being ‘Subpotent’
The respective product approval is based on Revlimid Capsules, 5mg, 10mg, 15mg, 25mg and 2.5mg, 20mg as a reference product
The transaction is expected to be completed in the second calendar quarter of 2025
While the litigation between Incyte Corporation and the company continues, the preliminary injunction is no longer in effect
The company will make the drug available under the brand name, PALENO (Palbociclib) 75 mg, 100 mg, 125 mg
The New Jersey-based unit of the Mumbai-based drug major is recalling Febuxostat Tablets in 40 mg and 80 mg strengths
USFDA conducted an inspection at Company’s Dadra facility from December 4, 2023 to December 15, 2023
This recognition attests to Sun Pharma’s commitment to incorporate Environmental, Social, and Governance principles through focused initiatives across its businesses
Ilumetri was approved for marketing in China in May 2023
The company initiated the Class II nationwide recall (US) on January 13 this year
Sun Pharmaceutical Industries Inc is recalling the affected lot due to ’Cross Contamination’
The health regulator inspected the manufacturing facility from April 26 to May 9, 2022
At the conclusion of the inspection, the USFDA issued a Form-483, with 8 observations
The company has entered into license agreement to commercialise a first-in-class innovative drug, Tyvalzi (Sovateltide) in India
With limited treatment options available to people living with severe alopecia areata in the U.S., the need for innovative therapies such as LEQSELVI remains critically important
At the conclusion of the inspection, the USFDA issued a Form-483, with 6 observations
Antibe is currently under court-observed liquidation proceedings
Within respective industries, this Yearbook aims to distinguish those companies that have demonstrated strengths in corporate sustainability
Bayer has granted the non-exclusive rights to Sun Pharma to market and distribute a second brand of Finerenone under the brand name Lyvelsa
The company initiated the Class II nationwide (US) recall on February 6, 2025
Princeton-based Sun Pharmaceutical Industries Inc is recalling the affected lot that was produced at the drugmaker’s Dadra-based facility
Sun Pharmaceutical will acquire 8,086,818 shares constituting 21.52% of the total outstanding shares of Taro for a cash consideration of $43 per share amounting to Rs 2,891.76 crore
Newly set up company will do localization of products which would be produced at prospective partners in China for sales locally
Earlier, TARO Pharmaceuticals Inc. had entered into an agreement with Antibe Therapeutics Inc.
SEZABY is a benzyl alcohol-free and propylene glycol-free formulation of phenobarbital sodium powder for injection
This strategic investment is to support development of innovative pharmaceutical delivery technologies and get access to the technology for certain molecules and territories
The company has entered into agreements to acquire minority stake in Agatsa Software and Remidio Innovative Solutions which are non-material investments by the Company in the allied areas
Concert is a late-stage biotechnology company pioneering the use of deuterium in medicinal chemistry
WINLEVI will be available in Canada this fall
The affected lot was manufactured at Sun Pharma’s Halol-based plant in Gujarat
The cost of acquisition is around $3.05 million
The total consolidated income of the company increased by 7.81% at Rs 13571.71 crore for Q4FY25
The company is recalling a generic drug indicated to raise blood pressure in adult patients with acute hypotension
CEQUA is the first dry eye treatment available in India that is delivered with nanomicellar (NCELL) technology
SEZABY is a benzyl alcohol-free and propylene glycol-free formulation of phenobarbital sodium powder for injection
Sun Pharmaceutical Industries’ partner Philogen S.p.A has voluntarily withdrawn the application for marketing authorization to the European Medicines Agency for Nidlegy
The said acquisition is expected to be completed by the end of May 2023
Total consolidated income of the company increased by 18.24% at Rs 11303.95 crore for Q4FY23
The company has entered into an agreement with US based Pharmazz Inc
The Uractiv portfolio comprises food supplements including minerals, vitamins and adjuvants; cosmetics and medical devices used for maintaining urinary tract health
WINLEVI works differently from any other topical acne treatment
Total consolidated income of the company increased by 9.29% at Rs 13645.39 crore for Q2FY25
The Mumbai-based drug major spent about Rs 2,400 crore on R&D in 2022-23
Under the indicative proposal, post the acquisition, Taro will become a wholly-owned subsidiary of Sun Pharma and will be delisted from NYSE
Post this acquisition, the Sun Pharma de Mexico, S.A. de C.V. would become a wholly-owned subsidiary of Sun Pharma
The company has acquired Disperzyme, Disperzyme-CD and Phlogam as part of the deal
The two partner companies will share post commercialization economics in about 50:50 ratio
Under the terms of this agreement, Zydus has granted Sun Pharma semi-exclusive rights to co-market the product in India
Total consolidated income of the company increased by 10.87% to Rs 11,414.85 crore for Q3FY23
Total consolidated income of the company increased by 10.65% at Rs 12630.90 crore for Q3FY24
Total consolidated income of the company increased by 11.96% at Rs 14141.08 crore for Q3FY25
The Mumbai-based company had reported a consolidated revenue of Rs 43,278 crore in 2022-23
Total consolidated income of the company increased by 10.73% at Rs 9560.35 crore for Q4FY22
The company, which posted revenues of Rs 38,426 crore in FY22, aims to invest 7-8 per cent of sales in the R&D front in the ongoing fiscal
Tildrakizumab Injection has also been approved for marketing in the US, EU, Japan, UK, Switzerland, Canada, Australia, Hong Kong