OneSource Specialty Pharma Allots 3,150 Equity Shares Under ESOP 2021, Paid-Up Capital Rises

1 min read     Updated on 13 May 2026, 03:08 PM
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OneSource Specialty Pharma Limited allotted 3,150 equity shares of INR 1/- each on May 13, 2026, under ONESOURCE ESOP 2021, following the exercise of vested options by eligible employees. The allotment raised the company's paid-up share capital from INR 114,642,651/- to INR 114,645,801/-, with total issued shares now at 11,46,45,801. The shares were issued at an exercise price of INR 278.00 per share, carrying a premium of INR 277.00 per share, and rank pari passu with existing equity shares. The disclosure was made under Regulation 30 of SEBI (Listing Obligations and Disclosures Requirements) Regulations, 2015.

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On May 13, 2026, OneSource Specialty Pharma Limited's Board of Directors approved the allotment of 3,150 equity shares of INR 1/- each under the OneSource Specialty Pharma Limited – Employee Stock Option Plan 2021 (ONESOURCE ESOP 2021). The allotment was made to eligible employees of the company upon exercise of vested options, in compliance with Regulation 30 of SEBI (Listing Obligations and Disclosures Requirements) Regulations, 2015. The newly issued shares rank pari passu with the existing equity shares of the company in all respects.

Impact on Paid-Up Share Capital

The allotment has resulted in an increase in the company's paid-up share capital. The following table summarises the change in share capital consequent to this allotment:

Metric: Before Allotment After Allotment
Paid-Up Share Capital: INR 114,642,651/- INR 114,645,801/-
Number of Equity Shares: 114,642,651 114,645,801
Face Value Per Share: INR 1/- INR 1/-

ESOP Allotment Details

The allotment has been made under the ONESOURCE ESOP 2021 scheme. Key details of the issuance, as disclosed under Regulation 10(c) of SEBI (Share Based Employee Benefits and Sweat Equity) Regulations, 2021, are presented below:

Parameter: Details
Scheme Name: OneSource Specialty Pharma Limited – Employee Stock Option Plan 2021
Kind of Security: Equity Shares
Par Value Per Share: INR 1/-
Date of Issue: May 13, 2026
Number of Shares Issued: 3,150
Distinctive Numbers: 125731972 to 125735121
Exercise Price Per Share: INR 278.00
Premium Per Share: INR 277.00
Total Issued Shares After Issue: 11,46,45,801
Total Issued Share Capital After Issue: INR 11,46,45,801/-
Lock-In Details: NA
Pari Passu with Existing Shares: Yes

Regulatory Compliance

The company filed the statement referred to in Regulation 10(b) of the SEBI (Share Based Employee Benefits) Regulations, 2021 with the stock exchanges on March 12, 2025. OneSource Specialty Pharma's shares are listed on both BSE Limited and the National Stock Exchange of India Limited. The disclosure was signed by Trisha A, Company Secretary and Compliance Officer (Membership Number: A47635), on behalf of the company.

Historical Stock Returns for Onesource Specialty Pharma

1 Day5 Days1 Month6 Months1 Year5 Years
+1.68%+4.38%+17.79%+5.44%+10.37%+6.43%

How many additional ESOP tranches are expected to vest under the ONESOURCE ESOP 2021 scheme in the coming quarters, and what is the potential dilution impact on existing shareholders?

Given the exercise price of INR 278 per share, how does this compare to OneSource Specialty Pharma's current market price, and what does this signal about employee sentiment toward the company's future growth prospects?

Will OneSource Specialty Pharma introduce a new ESOP scheme beyond 2021 to attract and retain talent as the company scales, and what size of employee stock pool might be considered?

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OneSource Backs Canada's Second Generic Semaglutide Approval in Key Market

2 min read     Updated on 04 May 2026, 08:43 AM
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OneSource Specialty Pharma supports its partner Orbicular in securing Health Canada approval for generic semaglutide injection, establishing the second generic approval in Canada's strategically important semaglutide market. The company will provide commercial supply from its US FDA-approved Bengaluru facility, reinforcing its global CDMO capabilities in complex drug-device combinations.

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OneSource Specialty Pharma announced that its partner Orbicular, along with its Canadian front-end partner, has received approval from Health Canada for a generic version of Ozempic® (semaglutide injection). This marks the second generic semaglutide approval in Canada, positioning OneSource partners as the first generic entrants in what is recognized as the world's second-largest semaglutide market.

Strategic Market Milestone

The latest regulatory approval represents a significant achievement for OneSource's expanding portfolio of complex pharmaceutical partnerships in one of the world's most important semaglutide markets. The milestone reflects a closely integrated development and manufacturing model where Orbicular led the product development and technical program for the complex peptide, while OneSource supported the program as the manufacturing partner.

Parameter: Details
Product: Generic Ozempic® (semaglutide injection)
Partner: Orbicular with Canadian front-end partner
Market Position: Second generic approval in Canada
Market Significance: World's second-largest semaglutide market
Regulatory Authority: Health Canada
Manufacturing Partner: OneSource Specialty Pharma

Manufacturing and Supply Chain Excellence

OneSource provided end-to-end manufacturing capabilities for the Canadian filing, with commercial supply to be supported from the company's US FDA-approved flagship facility in Bengaluru. The approval follows a recent tentative approval in the United States supported by OneSource, further reinforcing the company's growing presence in complex peptide-based injectable programs across highly regulated markets.

Manufacturing Details: Information
Supply Facility: US FDA-approved Bengaluru facility
Manufacturing Role: End-to-end manufacturing capabilities
Program Type: Complex drug-device-combination
Market Coverage: Highly regulated global markets

Global Market Expansion

The Canadian approval builds on momentum from India, where OneSource has been supplying multiple brands marketed by various partners following product launches in March. This strategic positioning establishes the company as a key player in the global semaglutide market across multiple jurisdictions, with particular strength in enabling first-to-market generic entries.

Mr. Neeraj Sharma, CEO & MD of OneSource Specialty Pharma Limited, commented: "We are pleased with these back-to-back approvals from two of our global customers in one of the most important semaglutide markets globally. This milestone reflects the strength of our CDMO platform, our compliance standards, technical expertise, and ability to scale complex drug-device-combination programs for highly regulated markets. Our partnership with Orbicular highlights our role in enabling global commercialization through strong, collaborative ecosystems."

CDMO Platform Capabilities

With a continued focus on complex drug-device combinations, biologics, and oral technology, OneSource is strengthening its position as a global CDMO partner. The company enables faster, reliable, and high-quality commercialization for partners worldwide through its comprehensive manufacturing and development capabilities across five state-of-the-art facilities.

Company Highlights: Details
Manufacturing Facilities: Five state-of-the-art facilities
Regulatory Approvals: Global regulatory authorities
Team Size: Over 1,600 professionals
Specialization: Complex pharmaceutical products
Focus Areas: Biologics, drug-device combinations, sterile injectables

Historical Stock Returns for Onesource Specialty Pharma

1 Day5 Days1 Month6 Months1 Year5 Years
+1.68%+4.38%+17.79%+5.44%+10.37%+6.43%

How will the entry of generic semaglutide competitors impact Novo Nordisk's Ozempic pricing strategy and market share in Canada?

What regulatory hurdles might OneSource face when seeking approvals for generic semaglutide in other major markets like Europe and Japan?

Could OneSource's success with complex peptide manufacturing attract partnerships with other major pharmaceutical companies developing GLP-1 receptor agonists?

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