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01 VIRCHOW LABORATORIES LIMITED. (1)
01 Sulfamethoxazole (1)
01 India (1)
60
PharmaCompass offers a list of Sulfamethoxazole 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 Sulfamethoxazole manufacturer or Sulfamethoxazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulfamethoxazole manufacturer or Sulfamethoxazole supplier.
PharmaCompass also assists you with knowing the Sulfamethoxazole API Price utilized in the formulation of products. Sulfamethoxazole API Price is not always fixed or binding as the Sulfamethoxazole Price is obtained through a variety of data sources. The Sulfamethoxazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 08D manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 08D, including repackagers and relabelers. The FDA regulates 08D manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 08D 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 08D manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 08D supplier is an individual or a company that provides 08D active pharmaceutical ingredient (API) or 08D finished formulations upon request. The 08D suppliers may include 08D API manufacturers, exporters, distributors and traders.
click here to find a list of 08D 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 08D Drug Master File in Japan (08D JDMF) empowers 08D 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 08D JDMF during the approval evaluation for pharmaceutical products. At the time of 08D 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 08D suppliers with JDMF on PharmaCompass.
