Core Viewpoint - North China Pharmaceutical announced that its wholly-owned subsidiary, North China Pharmaceutical Group Xiantai Pharmaceutical Co., Ltd., received a GMP compliance inspection notice from the Hebei Provincial Drug Administration for its sterile active pharmaceutical ingredient (API) production line [1] Group 1 - The inspection scope includes the sterile API (Piperacillin Sodium) production line 2 of the freeze-drying workshop 802 [1] - The inspection is scheduled from December 9 to December 12, 2025, and the conclusion indicates compliance with the Good Manufacturing Practice (GMP) requirements as per the 2010 revision [1] - The annual production capacity of the freeze-drying production line 2 is 150 tons, with a total investment of 74.5744 million yuan [1] Group 2 - This inspection marks the first GMP compliance check following the registration and filing of the newly added freeze-drying production line for Piperacillin Sodium [1]
华北制药:全资子公司通过药品GMP符合性检查