01 1DAEWOONG BIO INC.
02 2Inner Mongolia Changsheng Pharmaceutical Co. , Ltd.
03 1North China Pharmaceutical Group Semisyntech Co. , Ltd.
01 1Ampicillin
02 2Ampicillin hydrate
03 1[Japanese Pharmacopoeia] ampicillin
01 3China
02 1South Korea
[Japanese Pharmacopoeia] Ampicillin
Registration Number : 218MF11025
Registrant's Address : 12 BONGEUNSA-RO, 114-GIL, GANGNAM-GU, SEOUL, 135-715 KOREA
Initial Date of Registration : 2006-12-28
Latest Date of Registration : 2006-12-28
Registration Number : 307MF10054
Registrant's Address : Industry Zone, Tuoketuo, Hohhot, Inner Mongolia, China
Initial Date of Registration : 2025-04-16
Latest Date of Registration : 2025-04-16
Registration Number : 302MF10096
Registrant's Address : Industry Zone, Tuoketuo, Hohhot, Inner Mongolia, China
Initial Date of Registration : 2020-08-05
Latest Date of Registration : 2023-01-25
Registration Number : 301MF10028
Registrant's Address : No. 20 Yangzi Road, Shijiazhuang Economic and Technological Development Zone, Hebei 0...
Initial Date of Registration : 2019-07-05
Latest Date of Registration : 2019-07-05
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PharmaCompass offers a list of Ampicillin 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 Ampicillin manufacturer or Ampicillin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ampicillin manufacturer or Ampicillin supplier.
PharmaCompass also assists you with knowing the Ampicillin API Price utilized in the formulation of products. Ampicillin API Price is not always fixed or binding as the Ampicillin Price is obtained through a variety of data sources. The Ampicillin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Supen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Supen, including repackagers and relabelers. The FDA regulates Supen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Supen 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 Supen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Supen supplier is an individual or a company that provides Supen active pharmaceutical ingredient (API) or Supen finished formulations upon request. The Supen suppliers may include Supen API manufacturers, exporters, distributors and traders.
click here to find a list of Supen 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 Supen Drug Master File in Japan (Supen JDMF) empowers Supen 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 Supen JDMF during the approval evaluation for pharmaceutical products. At the time of Supen 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 Supen suppliers with JDMF on PharmaCompass.
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