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