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Tohoku Pharmaceutical: Dapoxetine hydrochloride, the raw material, passed CDE approval

 Last Update: 2021-09-20
 Source: Internet
 Author: User

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On August 26, Northeast Pharmaceutical issued an announcement stating that the company had recently inquired and learned on the platform of the “Registration Information Disclosure of APIs, Pharmaceutical Excipients and Packaging Materials” of the State Food and Drug Administration, and learned that the “Dapoxetine Hydrochloride” API registration application was passed Approved by CDE

Dapoxetine hydrochloride is a selective serotonin reuptake inhibitor (SSRIs) drug, mainly suitable for the treatment of premature ejaculation (PE) patients aged 18 to 64 years old

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