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Patient Awareness Material

(PDFs in English only)

Adverse Event Reporting : To report any adverse event or product quality complaint related to AstraZeneca product, write to patientsafety.india@astrazeneca.com

IN-8443 Approved for external use in December 2021 Expiration Date: 2/1/2023

Adverse Event Reporting : To report any adverse event or product quality complaint related to AstraZeneca product, write to patientsafety.india@astrazeneca.com

IN-8443 Approved for external use in December 2021 Expiration Date: 2/1/2023