01 1Biovet JSC
02 1ERCROS S. A.
03 1HEC PHARM CO. ,LTD
04 2Ningxia Qiyuan Pharmaceutical Co. , Ltd.
01 1Erythromycin
02 1Erythromycin Chioshianeito
03 3erythromycin
01 1Bulgaria
02 3China
03 1Spain
Registration Number : 217MF10893
Registrant's Address : 39 Petar Rakov Street 4550 Peshtera, Bulgaria
Initial Date of Registration : 2005-11-07
Latest Date of Registration : 2010-03-09
Registration Number : 218MF10942
Registrant's Address : Paseo del Deleite, s/n 28300 Aranjuez, Madrid Spain
Initial Date of Registration : 2006-11-24
Latest Date of Registration : 2006-11-24
Registration Number : 231MF10067
Registrant's Address : No. 62 Binjiang Road, Yidu, Hubei Province, P. R. China
Initial Date of Registration : 2019-03-11
Latest Date of Registration : 2019-03-11
Registration Number : 227MF10101
Registrant's Address : No. 1 Qiyuan Street, Wangyuan Industrial Area, Yinchuan City, Ningxia 750101, P. R. C...
Initial Date of Registration : 2015-04-09
Latest Date of Registration : 2015-04-09
Registration Number : 228MF10123
Registrant's Address : No. 1 Qiyuan Street, Wangyuan Industrial Area, Yinchuan City, Ningxia 750101, P. R. C...
Initial Date of Registration : 2016-07-06
Latest Date of Registration : 2016-07-06
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PharmaCompass offers a list of Erythromycin 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 Erythromycin manufacturer or Erythromycin supplier for your needs.
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PharmaCompass also assists you with knowing the Erythromycin API Price utilized in the formulation of products. Erythromycin API Price is not always fixed or binding as the Erythromycin Price is obtained through a variety of data sources. The Erythromycin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E5389_SIGMA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E5389_SIGMA, including repackagers and relabelers. The FDA regulates E5389_SIGMA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E5389_SIGMA 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 E5389_SIGMA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E5389_SIGMA supplier is an individual or a company that provides E5389_SIGMA active pharmaceutical ingredient (API) or E5389_SIGMA finished formulations upon request. The E5389_SIGMA suppliers may include E5389_SIGMA API manufacturers, exporters, distributors and traders.
click here to find a list of E5389_SIGMA 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 E5389_SIGMA Drug Master File in Japan (E5389_SIGMA JDMF) empowers E5389_SIGMA 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 E5389_SIGMA JDMF during the approval evaluation for pharmaceutical products. At the time of E5389_SIGMA 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 E5389_SIGMA suppliers with JDMF on PharmaCompass.
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