Aurobindo Pharma has received a final approval from the US Food
& Drug Administration (USFDA) to manufacture and market Tofacitinib Tablets, 5 mg and 10 mg, which is bioequivalent and therapeutically equivalent to the reference listed drug (RLD), Xeljanz Tablets, 5 mg
and 10 mg, of PF Prism C.V.
& Drug Administration (USFDA) to manufacture and market Tofacitinib Tablets, 5 mg and 10 mg, which is bioequivalent and therapeutically equivalent to the reference listed drug (RLD), Xeljanz Tablets, 5 mg
and 10 mg, of PF Prism C.V.
The product will be manufactured at APL Healthcare Unit IV, a wholly owned subsidiary of the company and will be launched immediately.
Disclaimer: No Business Standard Journalist was involved in creation of this content
First Published: Jun 04 2026 | 7:16 PM IST
