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, and more, enabling you to easily find the right Sulfamethoxazole manufacturer or Sulfamethoxazole supplier for your needs.
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A Sulfamethylisoxazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfamethylisoxazole, including repackagers and relabelers. The FDA regulates Sulfamethylisoxazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfamethylisoxazole 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 Sulfamethylisoxazole manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Sulfamethylisoxazole supplier is an individual or a company that provides Sulfamethylisoxazole active pharmaceutical ingredient (API) or Sulfamethylisoxazole finished formulations upon request. The Sulfamethylisoxazole suppliers may include Sulfamethylisoxazole API manufacturers, exporters, distributors and traders.
click here to find a list of Sulfamethylisoxazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Sulfamethylisoxazole Drug Master File in Japan (Sulfamethylisoxazole JDMF) empowers Sulfamethylisoxazole 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 Sulfamethylisoxazole JDMF during the approval evaluation for pharmaceutical products. At the time of Sulfamethylisoxazole 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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