Granules Pharmaceuticals, Inc received USFDA approval for Ramelteon Tablets, 8 mg
US Food & Drug Administration (US FDA) has approved the Abbreviated New Drug Application (ANDA) filed by Granules Pharmaceuticals, Inc (GPI)., a wholly owned foreign subsidiary of Granules India Limited for Ramelteon Tablets, 8 mg.
It is bioequivalent to the reference listed drug product (RLD), Rozerem Tablets, 8 mg, of Takeda Pharmaceuticals U.S.A., Inc. Ramelteon Tablets are used for the treatment of insomnia characterized by difficulty with sleep onset. Granules now has a total of 29 ANDA approvals from US FDA (27 Final approvals and 2 tentative approvals).
Ramelteon Tablets had U.S. sales of approximately million MAT for the most recent twelve months ending in June 2020 according to IQVIA Health.