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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A C10H11N3O3S manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C10H11N3O3S, including repackagers and relabelers. The FDA regulates C10H11N3O3S manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C10H11N3O3S 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 C10H11N3O3S manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A C10H11N3O3S supplier is an individual or a company that provides C10H11N3O3S active pharmaceutical ingredient (API) or C10H11N3O3S finished formulations upon request. The C10H11N3O3S suppliers may include C10H11N3O3S API manufacturers, exporters, distributors and traders.
click here to find a list of C10H11N3O3S 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 C10H11N3O3S Drug Master File in Japan (C10H11N3O3S JDMF) empowers C10H11N3O3S 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 C10H11N3O3S JDMF during the approval evaluation for pharmaceutical products. At the time of C10H11N3O3S 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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