Shijiazhuang Fourth Pharmaceutical’s moxifloxacin hydrochloride tablets have been approved.


Time:2022-01-24

On January 11, the moxifloxacin hydrochloride tablets (0.4g) developed by Shijiazhuang Sihua Pharmaceutical Co., Ltd. received a drug registration certificate issued by the National Medical Products Administration and are deemed to have passed the evaluation of consistency in quality and efficacy for generic drugs.
At the start of the new year, Shijiazhuang No.4 Pharmaceutical Company has once again delivered good news in its research and development efforts. On January 11, the moxifloxacin hydrochloride tablets (0.4g) developed by Shijiazhuang No.4 Pharmaceutical Co., Ltd. received a drug registration certificate issued by the National Medical Products Administration and are deemed to have passed the evaluation of consistency in quality and efficacy for generic drugs.
Previously, the moxifloxacin hydrochloride sodium injection developed by Shijiazhuang No.4 Pharmaceutical Company received approval from the National Medical Products Administration in 2020 and passed the evaluation of consistency in quality and efficacy for generic drugs. The recent approval of moxifloxacin hydrochloride tablets further strengthens the development of a comprehensive moxifloxacin product line.
It was introduced that moxifloxacin is a fourth-generation quinolone antibacterial agent and a new-generation antibiotic with a broad-spectrum antimicrobial profile. It is primarily used to treat various bacterial infections, including pneumonia, tuberculosis, endocarditis, conjunctivitis (pink eye), and respiratory tract infections.

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