01 1VIRCHOW LABORATORIES LIMITED.
01 1Sulfamethoxazole
01 1India
Registration Number : 302MF10036
Registrant's Address : Plot No. 4 to 10,S. V. Co-operative Indi. Estate,I. D. A. Jeedimetla,Hyderabad-500 05...
Initial Date of Registration : 2020-03-16
Latest Date of Registration : 2020-03-16
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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 SEPTRA DS manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SEPTRA DS, including repackagers and relabelers. The FDA regulates SEPTRA DS manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SEPTRA DS 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 SEPTRA DS manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SEPTRA DS supplier is an individual or a company that provides SEPTRA DS active pharmaceutical ingredient (API) or SEPTRA DS finished formulations upon request. The SEPTRA DS suppliers may include SEPTRA DS API manufacturers, exporters, distributors and traders.
click here to find a list of SEPTRA DS 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 SEPTRA DS Drug Master File in Japan (SEPTRA DS JDMF) empowers SEPTRA DS 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 SEPTRA DS JDMF during the approval evaluation for pharmaceutical products. At the time of SEPTRA DS 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 SEPTRA DS suppliers with JDMF on PharmaCompass.
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