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 UROPLUS DS-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UROPLUS DS-1, including repackagers and relabelers. The FDA regulates UROPLUS DS-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UROPLUS DS-1 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 UROPLUS DS-1 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A UROPLUS DS-1 supplier is an individual or a company that provides UROPLUS DS-1 active pharmaceutical ingredient (API) or UROPLUS DS-1 finished formulations upon request. The UROPLUS DS-1 suppliers may include UROPLUS DS-1 API manufacturers, exporters, distributors and traders.
click here to find a list of UROPLUS DS-1 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 UROPLUS DS-1 Drug Master File in Japan (UROPLUS DS-1 JDMF) empowers UROPLUS DS-1 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 UROPLUS DS-1 JDMF during the approval evaluation for pharmaceutical products. At the time of UROPLUS DS-1 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 UROPLUS DS-1 suppliers with JDMF on PharmaCompass.
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