01 2Changshan Seika Pharmaceutical (Jiangsu) Co., Ltd.
02 1Changzhou Qianhong Biopharma Co. , Ltd.
03 1Changzhou Tianpu Pharmaceutical Co., Ltd.
04 1Nanjing Jianyou Biochemical Pharmaceutical Co., Ltd.
05 1OPOCRIN S. p. A.
01 1Dalteparin Sodium
02 5Dalteparin sodium
01 4China
02 1Italy
03 1Blank
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 : 221MF10099
Registrant's Address : Nanjing High-tech Development Zone MA010-1
Initial Date of Registration : 2009-05-27
Latest Date of Registration : 2022-07-06
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A Nadroparin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nadroparin, including repackagers and relabelers. The FDA regulates Nadroparin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nadroparin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Nadroparin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nadroparin supplier is an individual or a company that provides Nadroparin active pharmaceutical ingredient (API) or Nadroparin finished formulations upon request. The Nadroparin suppliers may include Nadroparin API manufacturers, exporters, distributors and traders.
click here to find a list of Nadroparin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Nadroparin Drug Master File in Japan (Nadroparin JDMF) empowers Nadroparin 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 Nadroparin JDMF during the approval evaluation for pharmaceutical products. At the time of Nadroparin 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 Nadroparin suppliers with JDMF on PharmaCompass.
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