01 1ERCROS S. A.
01 1Erythromycin stearate
01 1Spain
Registration Number : 225MF10103
Registrant's Address : Paseo del Deleite, s/n 28300-Aranjuez, Madrid Spain
Initial Date of Registration : 2013-05-15
Latest Date of Registration : 2021-05-13
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PharmaCompass offers a list of Erythromycin Stearate 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 Stearate manufacturer or Erythromycin Stearate supplier for your needs.
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PharmaCompass also assists you with knowing the Erythromycin Stearate API Price utilized in the formulation of products. Erythromycin Stearate API Price is not always fixed or binding as the Erythromycin Stearate Price is obtained through a variety of data sources. The Erythromycin Stearate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A gallimycin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of gallimycin, including repackagers and relabelers. The FDA regulates gallimycin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. gallimycin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A gallimycin supplier is an individual or a company that provides gallimycin active pharmaceutical ingredient (API) or gallimycin finished formulations upon request. The gallimycin suppliers may include gallimycin API manufacturers, exporters, distributors and traders.
click here to find a list of gallimycin 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 gallimycin Drug Master File in Japan (gallimycin JDMF) empowers gallimycin 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 gallimycin JDMF during the approval evaluation for pharmaceutical products. At the time of gallimycin JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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