| Purpose | Announcement Date | Bonus Date | Record Date | Bonus Ratio |
|---|---|---|---|---|
| Bonus | 18 Sep 2025 | 3 Oct 2025 | 3 Oct 2025 | 1:1 |
| 1:1 Bonus Issue of Equity Shares Trading Members of the Exchange are hereby informed that SHILPA MEDICARE LTD has fixed Record Date for the purpose of Bonus Issue of Equity Shares of the Company. The transactions in the Equity Shares of the Company would be on an Ex-Bonus basis with effect from the under-mentioned date :- DEMATERIALISED SECURITIES - ROLLING SETTLEMENT SEGMENT COMPANY NAME & CODE SHILPA MEDICARE LTD. (530549) RECORD DATE 03/10/2025 PURPOSE Issue of 01 (ONE) Bonus Equity Shares of Re.1/- each for every 01 (ONE) existing Equity Share of Re.1/- each held. Ex-Bonus basis from Date & Sett. No. 03/10/2025 DR-728/2025-2026 Note : As informed by the company 9,77,90,908 Equity Shares would be allotted as on 06th October,2025 (Refer attached Companys Letter dated September 29, 2025) (As Per BSE Notice Dated on 29.09.2025) | ||||
USFDA conducted the Good Manufacturing Practices (GMP) inspection from October 24 to October 30 in 2024.
The certification came after a successful inspection by the Finnish Medicines Agency on behalf of EMA from March 10 to March 14, 2025
The partnership will work on a new biological entity (NBE) in the immuno-oncology field to better treat cancer.
Here are some of the stocks that may see significant price movement today: Aditya Birla Real Estate, Shilpa Medicare, Swiggy, etc.
No regulatory issues were raised by the USFDA at Unit-2 during the inspection, the company said in a regulatory filing.
Shilpa Medicare said it has completed Phase 3 trials for SMLNUD07 – Nor Ursodeoxycholic Acid (Nor UDCA) tablets in 165 NAFLD patients in India.
The certification followed a successful inspection by the European Medicines Agency, Austria, held from September 24 to September 26 at the Nacharam, Hyderabad facility.
This FDA approval is a milestone in cancer therapy as it presents a more convenient and precise alternative to the traditional tablet forms.
Shilpa Medicare is the first Indian company to gain approval for Phase III trials of Recombinant Human Albumin.
The European Directorate for the Quality of Medicines & Healthcare (EDQM) gave Shilpa Pharma Lifesciences, the company's subsidiary, the Certificate of Suitability (CEP) for Nifedipine.
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