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