NSEGeneral Updates16 Jul 2026 · 16 Jul 2026, 02:38 pm
General Updates
AstraZeneca Pharma India Limited · ASTRAZEN
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AstraZeneca Pharma India Limited has received permission from the Central Drugs Standard Control Organization to import and market Benralizumab 30 mg/ml solution for injection in pre-filled syringe (Fasenra) for an additional indication, Hypereosinophilic Syndrome (HES) in patients aged 12 years and older.
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AstraZeneca Pharma India Limited has informed the Exchange about General Updates
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ASTRAZEN_16072026143810_Intimation_to_Stock_Exchanges_Fasenra_HES_final.pdf
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July 16, 2026
The Manager- Listing
BSE Limited
Corporate Relationship Dept., 5th Floor, New Trading Ring
Rotunda Building, P J Towers, Dalal Street, Fort,
Mumbai - 400001
The Manager- Listing
National Stock Exchange of India Limited
Exchange Plaza, 5th Floor, Plot No. C/1, G Block
Bandra –Kurla Complex, Bandra (E),
Mumbai - 400051
Dear Sir,
Sub: Intimation under Regulation 30 of SEBI (Listing Obligations and Disclosure Requirements)
Regulation, 2015
This is to inform that on July 15, 2026, AstraZeneca Pharma India Limited has received permission
from the Central Drugs Standard Control Organization, Directorate General of Health Services,
Government of India to import for sale and distribution of Benralizumab 30 mg/ml solution for injection
in pre-filled syringe (Brand name: Fasenra®) for an additional indication.
Through this approval, Benralizumab is indicated for the treatment of patients aged 12 years and older
with Hypereosinophilic Syndrome (HES) without an identifiable non-haematologic secondary cause.
The receipt of this permission paves way for the marketing of Benralizumab 30 mg/ml solution for
injection in pre-filled syringe (Brand name: Fasenra®) in India for the specified additional indication,
subject to the receipt of related statutory approvals, if any.
We request you to take the above intimation on record.
Thanking you,
For AstraZeneca Pharma India Limited
Tanya Sanish
Company Secretary & Compliance Officer