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Dr. Reddy's API Offering

• Offers crystalline form-I i.e., Innovator form.
• The control strategy for the API impurity profile has been designed through quality-by- design (QbD) based development.
• Lactam impurity levels are not detected thus able to achieve USP/ EP compliance after milling - opening a possibility for a wide range of delivery systems like dispersible films, oral disintegrating tablets, etc.

We manufacture Pregabalin API at our cGMP API manufacturing facility, which was successfully inspected by international regulatory authorities - WHO GMP, KFDA, PMDA, ANVISA, and USFDA.

To know more about our API offerings, please read the Tech sheet on Pregabalin API by filling the contact form below.