01 1Andhra Organics Limited
01 1Trimethoprim
01 1India
Registration Number : 303MF10098
Registrant's Address : Plot No. 08,S. V Co-op. Industrial estate I. D. A, Jeedimetla,Hyderabad-500055,T. S, ...
Initial Date of Registration : 2021-06-22
Latest Date of Registration : 2024-05-15
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PharmaCompass offers a list of Trimethoprim 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 Trimethoprim manufacturer or Trimethoprim supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trimethoprim manufacturer or Trimethoprim supplier.
A Trisul manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trisul, including repackagers and relabelers. The FDA regulates Trisul manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trisul 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 Trisul manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Trisul supplier is an individual or a company that provides Trisul active pharmaceutical ingredient (API) or Trisul finished formulations upon request. The Trisul suppliers may include Trisul API manufacturers, exporters, distributors and traders.
click here to find a list of Trisul 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 Trisul Drug Master File in Japan (Trisul JDMF) empowers Trisul 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 Trisul JDMF during the approval evaluation for pharmaceutical products. At the time of Trisul 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 Trisul suppliers with JDMF on PharmaCompass.
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