01 1AARTI DRUGS LIMITED.
01 1TINIDAZOLE
01 1India
Registration Number : 221MF10180
Registrant's Address : Mahendra Industrial Estate, Ground floor, Plot no: 109-D, Road no: 29, Sion (E), Mumb...
Initial Date of Registration : 2009-08-07
Latest Date of Registration : 2009-08-07
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PharmaCompass offers a list of Tinidazole 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 Tinidazole manufacturer or Tinidazole supplier for your needs.
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PharmaCompass also assists you with knowing the Tinidazole API Price utilized in the formulation of products. Tinidazole API Price is not always fixed or binding as the Tinidazole Price is obtained through a variety of data sources. The Tinidazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 033KF7V46H manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 033KF7V46H, including repackagers and relabelers. The FDA regulates 033KF7V46H manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 033KF7V46H API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A 033KF7V46H supplier is an individual or a company that provides 033KF7V46H active pharmaceutical ingredient (API) or 033KF7V46H finished formulations upon request. The 033KF7V46H suppliers may include 033KF7V46H API manufacturers, exporters, distributors and traders.
click here to find a list of 033KF7V46H 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 033KF7V46H Drug Master File in Japan (033KF7V46H JDMF) empowers 033KF7V46H 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 033KF7V46H JDMF during the approval evaluation for pharmaceutical products. At the time of 033KF7V46H 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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