Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 1Alchem International Limited
02 2Alchem International Private Limited
03 1Santen Oy
01 1SENNOSIDES USP
02 1Sen'nosaido
03 2Sennoside
01 3India
02 1Japan
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Registration Number : 227MF10003
Registrant's Address : 201,Empire Plaza,Mehrauli-Gurgaon Road Sultanpur,New Delhi-110 030,INDIA
Initial Date of Registration : 2015-01-05
Latest Date of Registration : 2015-01-05
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Registration Number : 225MF10137
Registrant's Address : 201,Empire Plaza,Mehrauli-Gurgaon Road Sultanpur,New Delhi-110 030,INDIA
Initial Date of Registration : 2013-07-23
Latest Date of Registration : 2013-07-23
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Registration Number : 219MF10246
Registrant's Address : 301,Avalon Apartments,Mehrauli-Gurgaon Road Manglapuri,New Delhi-110 030,INDIA
Initial Date of Registration : 2007-07-17
Latest Date of Registration : 2007-07-17
Registration Number : 218MF10620
Registrant's Address : Niityhaankatu 20, FI-33720 Tampere, Finland
Initial Date of Registration : 2006-07-03
Latest Date of Registration : 2016-03-11
A Sennosides manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sennosides, including repackagers and relabelers. The FDA regulates Sennosides manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sennosides 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 Sennosides manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sennosides supplier is an individual or a company that provides Sennosides active pharmaceutical ingredient (API) or Sennosides finished formulations upon request. The Sennosides suppliers may include Sennosides API manufacturers, exporters, distributors and traders.
click here to find a list of Sennosides 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 Sennosides Drug Master File in Japan (Sennosides JDMF) empowers Sennosides 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 Sennosides JDMF during the approval evaluation for pharmaceutical products. At the time of Sennosides 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 Sennosides suppliers with JDMF on PharmaCompass.
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