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, and more, enabling you to easily find the right Ampicillin manufacturer or Ampicillin supplier for your needs.
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A Totapen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Totapen, including repackagers and relabelers. The FDA regulates Totapen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Totapen 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 Totapen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Totapen supplier is an individual or a company that provides Totapen active pharmaceutical ingredient (API) or Totapen finished formulations upon request. The Totapen suppliers may include Totapen API manufacturers, exporters, distributors and traders.
click here to find a list of Totapen 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 Totapen Drug Master File in Japan (Totapen JDMF) empowers Totapen 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 Totapen JDMF during the approval evaluation for pharmaceutical products. At the time of Totapen 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 Totapen suppliers with JDMF on PharmaCompass.
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