Healthcare
Small-cap - With a market cap of ₹504.30 Cr.
| EX-Date | Purpose |
|---|---|
| 28 04 2021 | Final Dividend & Audited Results |
| 22 07 2021 | Quarterly Results |
| 21 10 2021 | Quarterly Results |
| 20 01 2022 | Quarterly Results |
| 28 04 2022 | Audited Results & Dividend |
| 27 07 2022 | Quarterly Results |
| 14 11 2022 | Quarterly Results |
| 14 02 2023 | Quarterly Results |
| 26 04 2023 | Inter alia, to consider the issue of Secured, Redeemable, Non-Convertible Debentures on private placement basis, investment in securities to be issued by Biocon Biologics Limited and provision of guarantees/put options, amongst other matters. |
| 23 05 2023 | Final Dividend & Audited Results & A.G.M. |
| 10 08 2023 | Quarterly Results |
| 10 11 2023 | Quarterly Results |
| 08 02 2024 | Quarterly Results |
| 16 05 2024 | Audited Results & Final Dividend |
| 30 10 2024 | Quarterly Results |
| 27 01 2025 | Inter alia, to consider and approve:- (1) Raising of Funds through issuance of Commercial Papers (CPs) or through any other mode on private placement basis. |
| 30 01 2025 | Quarterly Results |
| 04 04 2025 | Inter alia, to consider and approve raising funds through issuance of Commercial Papers or through any other mode |
| 23 04 2025 | Inter alia, to consider and approve the proposal for raising of funds by way of issue of equity shares or any other eligible securities, through one or more of the permissible modes including but not limited to qualified institutions placement, rights issue, preferential issue, further public offer, etc. |
| 08 05 2025 | Final Dividend & Audited Results |
| 07 08 2025 | Quarterly Results |
| 01 10 2025 | Redemption(Part) of NCD Inter alia, it is proposed to consider early redemption of unlisted, secured, rated, redeemable, Non-Convertible Debentures (NCDs) of face value of INR 1,00,000/- each, issued and allotted by the Company on private placement basis on February 21, 2023, subject to approval of the Board of Directors of the Company proposed to be sought on October 01, 2025, and receipt of necessary approvals, on such date as may be determined by the Company. |
| 11 11 2025 | Quarterly Results |
Integrated Core Strategies (Asia) Pte purchased 80,61,599 shares at an average price of Rs 229.26 each share
At the conclusion of this inspection, the agency has issued Form 483s with 4 observations
Biocon Biologics and Amgen have executed the settlement agreement to resolve the pending patent litigation
The shares were sold at an average price of Rs 560 apiece, taking the transaction value at Rs 2,240 crore
The facility is acquired for a total consideration of $7.7 million
The transaction is completed on April 2, 2024
The approval further adds to Biocon’s portfolio of complex drug products
Clinical data showed that both Denosumab biosimilars have comparable quality, safety, and efficacy to the reference product
The inspection has been concluded with no observations
The approval is for the generic version of Victoza, indicated for the treatment of insufficiently controlled Type 2 Diabetes Mellitus
Biocon Biologics, which recently announced its acquisition of Viatris’ global biosimilars business, has secured multiple biosimilar approvals in the U.S., Europe, and over 100 countries across the globe
The Board of Directors at its meeting held on April 04, 2025, has approved the same
The company’s subsidiary has completed the integration of the acquired biosimilars business in over 70 countries
Biocon Pharma received tentative approval of its ANDA for Rivaroxaban Tablets USP, in 2.5 mg, 10 mg, 15 mg and 20 mg strengths
The market access agreements from numerous plans represent over 100+ million lives in the United States
At the conclusion of the inspection, the USFDA issued a Form 483 with five observations
The facility, spread across 340,000-square feet, will enhance capabilities manifold to manufacture drug substance of mAbs portfolio
Biocon will be responsible for obtaining regulatory approval for Liraglutide, and thereafter, for the manufacture and supply of the product in the Canadian market
As a result of the completion of this integration, Biocon Biologics is expected to grow its employee population to over 150 employees in North America
The approval will further strengthen Biocon’s portfolio of vertically integrated, complex drug products
Ustekinumab, a monoclonal antibody, is approved for the treatment of Psoriasis Vulgaris and Psoriatic Arthritis
Clinical data showed that both Denosumab biosimilars have comparable safety and efficacy to the reference product
The agreement aims to expand access and affordability of Insulin Aspart in the United States
There were no critical deficiencies and one deficiency cited under the category ‘Major’
Biocon Pharma in partnership with Carnegie Pharmaceuticals LLC, received tentative approval from USFDA
The company has sold a total of 21,789,164 shares, at an average price of Rs 560.04 apiece, in Syngene International
The total consolidated income of the company decreased by 11.95% at Rs 4,021.60 crore for Q1FY26
The Board of Directors of the company at its meeting held August 07, 2025, had considered and approved the same
The divestment of the non-core branded formulations business units in India is in line
This is based on a surveillance inspection conducted by the agency between September 23 to 27, 2024
Consolidated total income of the company increased by 49.66% at Rs 4,519.20 crore for Q3FY24
The agreement is effective from January 1, 2024 and commercialisation commenced on February 1, 2024
The said Bangalore facility went under an EU GMP inspection in February 2023
The total consolidated income of the company increased by 12.31% at Rs 4,453.90 crore for Q4FY25
The approval of JOBEVNE expands Biocon Biologics’ biosimilar oncology portfolio in the United States
Post this transaction, the shareholding of the Company in Syngene shall stand at 52.46%
Consideration received from such sale/disposal is Rs 366 crore including working capital adjustments
The approval will further strengthen Biocon’s portfolio of vertically integrated, complex drug products
The company initiated the Class II recall on March 17, 2025
Total consolidated income of the company increased by 58.57% at Rs 3516.10 crore for Q1FY24
Biocon was the first and only pharmaceutical company from India to be featured on the ASIA IP ELITE list in 2016
This investment helps Biocon diversify its manufacturing base, strengthen its supply chain and accelerate the expansion of its global footprint
Thereby, Bicara will cease to be an associate company of Biocon
This relates to the cGMP inspection conducted by the agency between September 15 - 27, 2024
The investment will help Biocon Biologics’ acquisition of the biosimilars business of its partner Viatris
This agreement enables the company to launch ‘YESAFILI’ in the United States in the second half of calendar year 2026 or earlier in certain circumstances
The study will cover several tertiary hospitals specialized in handling UC cases
As a part of this collaboration, Biocon Biologics will continue to leverage Eris’ strong commercial footprint to significantly expand patient access to its world class biosimilars in India
Total consolidated income of the company increased by 22.56% at Rs 2384.20 crore for Q2FY23
The Board of Directors at its meeting held on November 14, 2022, inter alia, has approved the same
KIRSTY will be available as a single-patient-use prefilled pen for subcutaneous use and a multiple-dose vial for subcutaneous and intravenous use
The Fund Raising Committee of the company at its meeting held on June 16, 2025 authorised the opening of the issue
Under the terms of this deal, Yoshindo gets exclusive commercialization rights in Japan for bUstekinumab and bDenosumab developed and manufactured by Biocon Biologics
The collaboration is to include a new Insulin Glargine medicine that will benefit patients in the United States by increasing supply of high-quality affordable insulins
Biomm is Brazil’s first and only biotechnology focused company, providing high quality healthcare to patients with chronic conditions and enhancing access to the latest technologies and treatments
Earlier in 2023, over 70 Emerging Markets were integrated in July, the North America business transitioned in September and the European business in November
YESINTEK is intended for the treatment of adults and children with plaque psoriasis and adults with psoriatic arthritis or Crohn’s disease
The OAI status may cause delay and/or withholding of pending product approvals or supplements from the facility
In addition, the USFDA granted provisional interchangeability designation for both BOSAYA and AUKELSO
The lot has been manufactured by Biocon Pharma and distributed in the US by Iselin-based Biocon Pharma Inc
Biocon’s S&P Global ESG score was 63 versus 52 previously
The centralized marketing authorization granted by the EC is valid in all EU Member States as well as in the European Economic Area (EEA) countries Iceland, Liechtenstein and Norway
Biocon Biologics is among the Top 50 Companies among 175 participating companies to feature on this prestigious list
Date of maturity of the said NCDs will be on February 21, 2028
Three observations were cited at the end of the inspection, which the company will be addressing within the stipulated time
These inspections were conducted between July 10, 2023 and July 20, 2023
Debt facility agreement which is classified as a Sustainability-linked Loan amounting to $1.2 billion on November 20, 2022
Maturity of the said Commercial Papers will be on September 30, 2025
The maturity date of the said commercial papers was February 22, 2023
Since receiving EU marketing authorization in 2020, Nepexto has earned broad adoption across Europe
Yesintek and Yesintek I.V. are indicated for the treatment of moderate to severe plaque psoriasis in adult patients and in pediatric patients
The Board of Directors at its meeting held on April 23, 2025, has inter-alia, considered and approved the same
The approval is for the generic versions of Victoza to treat Type-2 Diabetes and Saxenda used in the treatment of weight management
The company has received an order of adjudication imposing a penalty dated February 22, 2024, from the office of Deputy Commissioner of Commercial Taxes, Divisional GST Office, Bangalore
The company has received award for its Oral Cancer Screening Program by IHW Council
This collaboration combines the company’s expertise in biosimilars with NCSM’s community outreach to enhance cancer care accessibility and affordability in Malaysia
The approval further adds to Biocon’s portfolio of complex drug products
Total consolidated income of the company increased by 58.67% at Rs 3928.80 crore for Q4FY23
Under the terms of this agreement Biocon will be responsible for the manufacturing and supply of Liraglutide to Zentiva, for its commercialization across 30 countries in Europe
Date of maturity of said Commercial Papers will be February 22, 2023
Yesintek will be available in all the same formulations currently provided by Stelara
BBL will have access to 100 million doses of vaccines annually together with the distribution rights to Serum’s Vaccine portfolio
Clinical data from the trial program demonstrated that our Ustekinumab biosimilar has comparable safety and efficacy to the originator product
Biocon achieved an ESG Score of 76 in the Environmental Dimension, 74 in the Social Dimension, and 62 in the Governance & Economic Dimension
This approval paves the way for the launch of YESAFILI in Canada, scheduled for July 4, 2025
Sitagliptin tablets are indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus
The drug-device combination will be marketed in the U.K. under the brand names Liraglutide Biocon for diabetes (gVictoza) and Biolide for chronic weight management (gSaxenda)
Biocon Biologics was recognized as the winner as it garnered the maximum number of votes from among 70,000 biopharma professionals who participated in the survey
Liraglutide is a drug-device combination formulation used in the treatment of Type 2 Diabetes Mellitus
This approval reflects Biocon Biologics’ compliance with the highest international regulatory standards
This achievement reinforces Biocon Biologics’ long-standing commitment to advancing diabetes care and ensuring affordable access to insulin across the country
With this acquisition Biocon Biologics emerges as a world leading biosimilars player with eight commercialized products
The full transition of Viatris’ biosimilars operations to Biocon Biologics in Europe represents another significant milestone as a world-leading biosimilars company
USFDA had conducted the said an inspection between September 23-27, 2024
USFDA had conducted the said an inspection between September 17-27, 2024
Total consolidated income of the company decreased by 14.67% at Rs 3856.20 crore for Q3FY25
Post this purchase, Biocon’s stake in BBL will be 90.2%
Biocon has been ranked 8th on the list this year for three key attributes: ‘innovative leader in the industry’, ‘is socially responsible’ and ‘has loyal employees
Total consolidated income of the company increased by 0.07% at Rs 3622.90 crore for Q2FY25
This relates to the cGMP inspection conducted by the agency between February 20- 28, 2024





