01 1Alembic Pharmaceuticals Limited
01 1Azithromycin Dihydrate
01 1India
Registration Number : 306MF10146
Registrant's Address : Alembic Road, Vadodara 390 003, Gujarat, India
Initial Date of Registration : 2024-11-20
Latest Date of Registration : 2024-11-20
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PharmaCompass offers a list of Azithromycin Dihydrate 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 Azithromycin Dihydrate manufacturer or Azithromycin Dihydrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Azithromycin Dihydrate manufacturer or Azithromycin Dihydrate supplier.
PharmaCompass also assists you with knowing the Azithromycin Dihydrate API Price utilized in the formulation of products. Azithromycin Dihydrate API Price is not always fixed or binding as the Azithromycin Dihydrate Price is obtained through a variety of data sources. The Azithromycin Dihydrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ribotrex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ribotrex, including repackagers and relabelers. The FDA regulates Ribotrex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ribotrex 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 Ribotrex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ribotrex supplier is an individual or a company that provides Ribotrex active pharmaceutical ingredient (API) or Ribotrex finished formulations upon request. The Ribotrex suppliers may include Ribotrex API manufacturers, exporters, distributors and traders.
click here to find a list of Ribotrex 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 Ribotrex Drug Master File in Japan (Ribotrex JDMF) empowers Ribotrex 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 Ribotrex JDMF during the approval evaluation for pharmaceutical products. At the time of Ribotrex 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 Ribotrex suppliers with JDMF on PharmaCompass.
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