01 1BGP Healthcare Pvt. Ltd
02 1Siegfried Ltd
01 2Nicotine
01 1India
02 1Switzerland
Registration Number : 303MF10099
Registrant's Address : Plot No. 3707, GIDC, Ankleshwar 393 002, Bharuch Dist. Gujarat State, India
Initial Date of Registration : 2021-07-01
Latest Date of Registration : 2022-10-26
Registration Number : 219MF10004
Registrant's Address : Untere Bru(¨)hlstrasse 4,CH-4800 Zofingen Switzerland
Initial Date of Registration : 2007-01-18
Latest Date of Registration : 2016-12-26
A Nicotine Hydrogen Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nicotine Hydrogen Tartrate, including repackagers and relabelers. The FDA regulates Nicotine Hydrogen Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nicotine Hydrogen Tartrate 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 Nicotine Hydrogen Tartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nicotine Hydrogen Tartrate supplier is an individual or a company that provides Nicotine Hydrogen Tartrate active pharmaceutical ingredient (API) or Nicotine Hydrogen Tartrate finished formulations upon request. The Nicotine Hydrogen Tartrate suppliers may include Nicotine Hydrogen Tartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Nicotine Hydrogen Tartrate 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 Nicotine Hydrogen Tartrate Drug Master File in Japan (Nicotine Hydrogen Tartrate JDMF) empowers Nicotine Hydrogen Tartrate 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 Nicotine Hydrogen Tartrate JDMF during the approval evaluation for pharmaceutical products. At the time of Nicotine Hydrogen Tartrate 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 Nicotine Hydrogen Tartrate suppliers with JDMF on PharmaCompass.
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