01 1High Tech Pharm Co. , Ltd.
02 1JW Pharmaceutical Corporation
01 2Imipenem hydrate
01 2South Korea
Registration Number : 304MF10138
Registrant's Address : 12, Cheomdansaneop 6-ro, Daesowon-myeon, Chungju-si, Chungcheongbuk-do, 27466, Korea
Initial Date of Registration : 2022-10-05
Latest Date of Registration : 2022-10-05
Registration Number : 219MF10002
Registrant's Address : 2477, Nambusunhwan-ro Seocho-gu, Seoul, Republic of Korea
Initial Date of Registration : 2007-01-18
Latest Date of Registration : 2012-05-11
77
PharmaCompass offers a list of Imipenem 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 Imipenem manufacturer or Imipenem supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Imipenem manufacturer or Imipenem supplier.
PharmaCompass also assists you with knowing the Imipenem API Price utilized in the formulation of products. Imipenem API Price is not always fixed or binding as the Imipenem Price is obtained through a variety of data sources. The Imipenem Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 64221-86-9 (Parent) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 64221-86-9 (Parent), including repackagers and relabelers. The FDA regulates 64221-86-9 (Parent) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 64221-86-9 (Parent) 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 64221-86-9 (Parent) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 64221-86-9 (Parent) supplier is an individual or a company that provides 64221-86-9 (Parent) active pharmaceutical ingredient (API) or 64221-86-9 (Parent) finished formulations upon request. The 64221-86-9 (Parent) suppliers may include 64221-86-9 (Parent) API manufacturers, exporters, distributors and traders.
click here to find a list of 64221-86-9 (Parent) 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 64221-86-9 (Parent) Drug Master File in Japan (64221-86-9 (Parent) JDMF) empowers 64221-86-9 (Parent) 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 64221-86-9 (Parent) JDMF during the approval evaluation for pharmaceutical products. At the time of 64221-86-9 (Parent) 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 64221-86-9 (Parent) suppliers with JDMF on PharmaCompass.
We have 2 companies offering 64221-86-9 (Parent)
Get in contact with the supplier of your choice:
