As understood, there should be the complete stability data submitted along with the registration dossier or before the registration approval in your country, but the study batches might be not the pilot batch (not production/commercial batch).
Thus we would like to propose you to
• Provide us the stability data of which had been submitted to Indian FDA for registration application in INDIA.
We can use the such information instead of the complete stability data of production batch.
• If possible, please also provide us the stability data of the production/commercial batch even though it is not yet completed.