BSECompany Update10 Aug 2026 · 10 Aug 2026, 06:02 pm
Lupin Announces the Approval of Sodium Zirconium Cyclosilicate for Oral Suspension in the United States.
Lupin Ltd · 500257
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Lupin Ltd has received approval from the US FDA for its Abbreviated New Drug Application for Sodium Zirconium Cyclosilicate for Oral Suspension, which is indicated for the treatment of hyperkalemia in adults.
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Lupin Ltd - 500257 - Announcement under Regulation 30 (LODR)-Press Release / Media Release
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August 10, 2026
National Stock Exchange of India Limited BSE Limited
Exchange Plaza, P. J. Towers, Dalal Street,
Bandra Kurla Complex, Mumbai Samachar Marg,
Bandra (East), Mumbai - 400 001
Mumbai - 400 051
Symbol: LUPIN Scrip Code: Equity - 500257
Subject: Disclosure pursuant to Regulation 30 of the Securities and Exchange Board of India
(Listing Obligations and Disclosure Requirements) Regulations, 2015
Dear Sir/Madam,
We are pleased to enclose a Press Release titled “Lupin Announces the Approval of Sodium Zirconium Cyclosilicate
for Oral Suspension in the United States”.
The same is for your information and dissemination.
Thanking you,
For LUPIN LIMITED
AMIT KUMAR GUPTA
COMPANY SECRETARY & COMPLIANCE OFFICER
(ACS -15754)
Encl.: a/a.
LUPIN LIMITED
Registered Office: 3rd Floor, Kalpataru Inspire, Off W. E. Highway, Santacruz (East), Mumbai - 400 055 India. Tel: (91-22) 6640 2323.
Corporate Identity Number: L24100MH1983PLC029442 info@lupin.com | www.lupin.com
Press Release
BSE: 500257 NSE: LUPIN REUTERS: LUPIN.BO BLOOMBERG: LPCIN
Lupin Announces the Approval of Sodium Zirconium Cyclosilicate for Oral Suspension
in the United States
Mumbai, India, Naples, Fla, August 10, 2026: Global pharma major Lupin Limited (Lupin) today announced
that it has received approval from the U.S. Food and Drug Administration (U.S. FDA) for its Abbreviated
New Drug Application for Sodium Zirconium Cyclosilicate for Oral Suspension, 5 g/packet and 10 g/packet.
The U.S. FDA has approved Lupin’s Sodium Zirconium Cyclosilicate for Oral Suspension, 5 g/packet and
10 g/packet as bioequivalent to the reference listed drug (RLD) Lokelma® for Oral Suspension of
AstraZeneca Pharmaceuticals LP and is indicated for the treatment of hyperkalemia in adults.
Sodium Zirconium Cyclosilicate for Oral Suspension (RLD Lokelma®) had estimated annual sales of USD 568
million in the U.S. (IQVIA MAT Jun 2026).
About Lupin
Lupin Limited is a global pharmaceutical leader headquartered in Mumbai, India, with a strong presence across
India, the U.S., Other Developed Markets, and Emerging Markets, with products distributed in over 100 markets.
Lupin has a diversified portfolio spanning generics, complex generics, specialty medicines, and biosimilars, and
continues to strengthen its market position through a differentiated portfolio. The company maintains strong
leadership in the U.S. and India across core therapeutic areas, including cardiovascular, respiratory, diabetes,
gastrointestinal, and women’s health. 15 state-of-the-art manufacturing facilities support sustainable operations,
with 6 research centers and a dedicated workforce of over 26,000 professionals. Lupin continues to expand the
healthcare ecosystem through diagnostics, digital health, patient-support programs, and disease management
initiatives. Sustainability continues to be a core pillar of the company’s business strategy.
To know more, visit www.lupin.com or follow us on LinkedIn https://www.linkedin.com/company/lupin
For further information or queries, please contact:
Rajalakshmi Azariah
Vice President & Global Head – Corporate Communications, Lupin
rajalakshmiazariah@lupin.com
Elise Titan
Director – U.S. Communications, Lupin
elisetitan@lupin.com
Safe Harbor Statement
Lokelma® is a registered trademark of ZS Pharma, Inc.
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