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See the DrugPatentWatch profile for Glyxambi
Glyxambi (empagliflozin/linagliptin) received European Medicines Agency (EMA) approval on 22 August 2014. [1]
The EMA authorization was for Glyxambi, a fixed-dose combination of empagliflozin and linagliptin for use in type 2 diabetes mellitus. [1]
Yes. The EMA date refers to the marketing authorization approval date by the agency (22 August 2014 for Glyxambi), which is different from when the product became available in specific EU/EEA markets. [1]
[1] https://www.ema.europa.eu/en/medicines/human/EPAR/glyxambi
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