Healthcare
Small-cap - With a market cap of ₹216.47 Cr.
EX-Date | Purpose |
---|---|
25 05 2021 | Audited Results |
09 08 2021 | Quarterly Results & Interim Dividend |
09 11 2021 | Quarterly Results |
08 02 2022 | Quarterly Results |
26 05 2022 | Final Dividend & Audited Results |
08 08 2022 | Quarterly Results |
11 11 2022 | Quarterly Results |
10 02 2023 | Quarterly Results |
30 05 2023 | Dividend & Audited Results |
14 08 2023 | Quarterly Results |
09 11 2023 | Quarterly Results |
08 02 2024 | Quarterly Results |
13 11 2024 | Quarterly Results |
11 02 2025 | Quarterly Results |
30 05 2025 | Dividend & Audited Results |
Through this approval, Tremelimumab (Imjudo) in combination with Durvalumab (Imfinzi) is indicated for the treatment of patients with unresectable hepatocellular carcinoma
The company has received approval from Central Drugs Standard Control Organisation
Durvalumab in combination with Tremelimumab is indicated for the treatment of patients with unresectable hepatocellular carcinoma
Trastuzumab deruxtecan is indicated for the treatment of adult patients with unresectable or metastatic HER2-positive breast cancer who have received a prior anti-HER2-based regimen
The receipt of this permission paves way for the marketing of Osimertinib Tablets 40 mg & 80 mg in India for the specified additional indication
Through this approval, Sodium Zirconium Cyclosilicate is indicated for the treatment of hyperkalaemia in adult patients
Eculizumab (Soliris) is indicated for the treatment of patients with PNH and aHUS to inhibit complement
Earlier, the company had received Import and Market Permission in Form CT-20 from the Drugs Controller General of India for Selumetinib (Koselugo)
AstraZeneca will retain the intellectual property rights to budesonide and formoterol fumarate dihydrate and will continue to be the Marketing Authorisation Holder and import license
The company had received marketing authorisation for Olaparib film-coated tablets 100mg and 150mg (Lynparza) on November 17, 2023
The company has received permission from the Central Drugs Standard Control Organisation, Directorate General of Health Services, Government of India
The Company will position the manufacturing site for sale in a fully operational manner
In December 2023, the company had received import and market permission in Form CT-20 from the Drugs Controller General of India for Breztri Aerosphere
The company has received permission from Central Drugs Standard Control Organisation
Enhertu is indicated for the treatment of adult patients with unresectable or metastatic HER2-positive breast cancer who have received a prior anti-HER2-based regimen
The receipt of this permission paves way for the launch of Olaparib film coated tablets of 100mg/150mg (Lynparza) in India
The receipt of this permission paves way for the launch of Durvalumab 120 mg/2.4 mL and 500 mg/10 mL solution for infusion (Imfinzi) in India for the specified additional indication
Through this approval, Dapagliflozin Tablets 10mg is indicated for the treatment of heart failure in adults
The company has received permission from the Central Drugs Standard Control Organisation
The receipt of this permission paves way for the launch of Forxiga tablets of 10 mg in India for the specified additional/expanded indication
The company has received permission from the CDSCO to import for sale and distribution of Osimertinib Tablets 40 mg & 80 mg (TAGRISSO) for an additional indication
Benralizumab is indicated as an add-on treatment for adult patients with relapsing or refractory eosinophilic granulomatosis with polyangiitis