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