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01 1Biovet JSC
02 1ERCROS S. A.
03 1HEC PHARM CO. ,LTD
04 2Ningxia Qiyuan Pharmaceutical Co. , Ltd.
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01 1Erythromycin
02 1Erythromycin Chioshianeito
03 3erythromycin
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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 : 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
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
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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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Erythromycin manufacturer or Erythromycin supplier.
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 Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard, including repackagers and relabelers. The FDA regulates Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard 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 Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard supplier is an individual or a company that provides Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard active pharmaceutical ingredient (API) or Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard finished formulations upon request. The Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard suppliers may include Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard API manufacturers, exporters, distributors and traders.
click here to find a list of Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard 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 Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard Drug Master File in Japan (Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard JDMF) empowers Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard 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 Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard JDMF during the approval evaluation for pharmaceutical products. At the time of Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard 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 Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard suppliers with JDMF on PharmaCompass.
We have 4 companies offering Erythromycin, for microbiological assay, European Pharmacopoeia (EP) Reference Standard
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