Two new products from the company have received drug production registration approvals.


Time:2019-01-08

The hydrochloride ambroxol injection in three-in-one polypropylene (PP) plastic ampoules—available in 4 ml: 30 mg, 2 ml: 15 mg, and 1 ml: 7.5 mg—and the tirofiban hydrochloride sodium injection in glass bottles (250 ml and 100 ml)—both developed by the company over a period of five years—have obtained drug production registration approvals from the National Medical Products Administration.
Recently, the ambroxol hydrochloride injection—available in three formulations packaged in combined polypropylene (PP) plastic ampoules (including 4 ml: 30 mg, 2 ml: 15 mg, and 1 ml: 7.5 mg)—and the tirofiban hydrochloride sodium injection—available in glass bottles (250 ml and 100 ml)—both developed by the company over a period of five years, have received drug production registration approvals from the National Medical Products Administration.
According to information obtained from the company’s Drug Research Institute, Ambroxol Hydrochloride Injection belongs to Category 6 of original chemical drugs and is used for the treatment of respiratory diseases. Tirofiban Hydrochloride Sodium Injection also belongs to Category 6 of original chemical drugs; it is a cardiovascular medication indicated for the treatment of patients with non-ST-segment elevation acute coronary syndromes (NSTE-ACS).

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