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, Price,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.
PharmaCompass also assists you with knowing the Trimethoprim API Price utilized in the formulation of products. Trimethoprim API Price is not always fixed or binding as the Trimethoprim Price is obtained through a variety of data sources. The Trimethoprim Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Resprim Forte manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Resprim Forte, including repackagers and relabelers. The FDA regulates Resprim Forte manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Resprim Forte 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 Resprim Forte manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Resprim Forte supplier is an individual or a company that provides Resprim Forte active pharmaceutical ingredient (API) or Resprim Forte finished formulations upon request. The Resprim Forte suppliers may include Resprim Forte API manufacturers, exporters, distributors and traders.
click here to find a list of Resprim Forte 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 Resprim Forte Drug Master File in Japan (Resprim Forte JDMF) empowers Resprim Forte 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 Resprim Forte JDMF during the approval evaluation for pharmaceutical products. At the time of Resprim Forte 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 Resprim Forte suppliers with JDMF on PharmaCompass.
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