Two New Products of the Company Receive Drug Production Registration Approvals
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发布时间:2019-01-08
【概要描述】
After five years of development by the company, the ambroxol hydrochloride injection in three-in-one polypropylene (PP) ampoule packaging—available in 4 mL: 30 mg, 2 mL: 15 mg, and 1 mL: 7.5 mg—and the tirofiban hydrochloride sodium chloride injection in glass vial packaging—available in 250 mL and 100 mL—have both obtained drug production registration approvals from the National Medical Products Administration.
Recently, the company’s five-year development of a three-in-one polypropylene (PP) ampoule packaging for ambroxol hydrochloride injection—available in 4 mL: 30 mg, 2 mL: 15 mg, and 1 mL: 7.5 mg—and glass-bottle packaging for tirofiban hydrochloride sodium chloride injection—in 250 mL and 100 mL sizes—has been granted drug production registration approval by the National Medical Products Administration.
According to the company’s Pharmaceutical Research Institute, ambroxol hydrochloride injection is classified as a Category 6 original chemical drug and is indicated for the treatment of respiratory diseases. Tirofiban hydrochloride sodium chloride injection is also classified as a Category 6 original chemical drug and is a cardiovascular medication used in the management of patients with non-ST-segment elevation acute coronary syndrome (NSTE-ACS).
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