01 2Changshan Seika Pharmaceutical (Jiangsu) Co., Ltd.
02 1Changzhou Qianhong Biopharma Co. , Ltd.
03 1Changzhou Tianpu Pharmaceutical Co., Ltd.
04 1Hebei Changshan Biochemical Pharmaceutical Co. , Ltd.
05 1Nanjing Jianyou Biochemical Pharmaceutical Co., Ltd.
06 1OPOCRIN S. p. A.
01 1Dalteparin Sodium
02 6Dalteparin sodium
01 4China
02 1Italy
03 2Blank
Registration Number : 223MF10084
Registrant's Address : No. 18 Guoxiang Road, Wujin Economic Development Zone, Changzhou City, Jiangsu Provin...
Initial Date of Registration : 2011-06-17
Latest Date of Registration : 2019-01-10
Registration Number : 301MF10042
Registrant's Address : No. 18 Guoxiang Road, Wujin Economic Development Zone, Changzhou City, Jiangsu Provin...
Initial Date of Registration : 2019-08-09
Latest Date of Registration : 2019-08-09
Registration Number : 218MF10583
Registrant's Address : No. 1, Changhong West Road, Hutang Town, Wujin District, Changzhou City, Jiangsu Prov...
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2009-12-25
Registration Number : 219MF10099
Registrant's Address : No. 192 Huanghe West Rd. Xinbei District Changzhou, Jiangsu, China
Initial Date of Registration : 2007-03-14
Latest Date of Registration : 2014-05-21
Registration Number : 227MF10152
Registrant's Address : Via Pacinotti, 3 41043 Corlo di Formigine (Modena) Italy
Initial Date of Registration : 2015-06-01
Latest Date of Registration : 2015-06-01
Registration Number : 308MF10011
Registrant's Address : No. 71, Menglong Street, South District of Zhengding High-tech Industrial Development...
Initial Date of Registration : 2026-01-08
Latest Date of Registration : 2026-01-08
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Product Web Link
Virtual Booth
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Website
Corporate PDF
Registration Number : 221MF10099
Registrant's Address : Nanjing High-tech Development Zone, Site MA010-1
Initial Date of Registration : 2009-05-27
Latest Date of Registration : 2022-07-06
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Dalteparin sodium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Dalteparin sodium manufacturer or Dalteparin sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dalteparin sodium manufacturer or Dalteparin sodium supplier.
A Liquaemin Lock Flush manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liquaemin Lock Flush, including repackagers and relabelers. The FDA regulates Liquaemin Lock Flush manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liquaemin Lock Flush API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Liquaemin Lock Flush supplier is an individual or a company that provides Liquaemin Lock Flush active pharmaceutical ingredient (API) or Liquaemin Lock Flush finished formulations upon request. The Liquaemin Lock Flush suppliers may include Liquaemin Lock Flush API manufacturers, exporters, distributors and traders.
click here to find a list of Liquaemin Lock Flush suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Liquaemin Lock Flush Drug Master File in Japan (Liquaemin Lock Flush JDMF) empowers Liquaemin Lock Flush API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Liquaemin Lock Flush JDMF during the approval evaluation for pharmaceutical products. At the time of Liquaemin Lock Flush JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Liquaemin Lock Flush suppliers with JDMF on PharmaCompass.
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