01 Changshan Seika Pharmaceutical (Jiangsu) Co., Ltd. (2)
02 Changzhou Qianhong Biopharma Co. , Ltd. (1)
03 Changzhou Tianpu Pharmaceutical Co., Ltd. (1)
04 Nanjing Jianyou Biochemical Pharmaceutical Co., Ltd. (1)
05 OPOCRIN S. p. A. (1)
01 Dalteparin Sodium (1)
02 Dalteparin sodium (5)
01 China (4)
02 Italy (1)
03 Blank (1)
20
PharmaCompass offers a list of Dalteparin sodium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,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.
PharmaCompass also assists you with knowing the Dalteparin sodium API Price utilized in the formulation of products. Dalteparin sodium API Price is not always fixed or binding as the Dalteparin sodium Price is obtained through a variety of data sources. The Dalteparin sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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.
We have 4 companies offering Nadroparin
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