Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 1Alchem International Private Limited
02 1Boehringer Ingelheim Pharma GmbH & Co. K.G.
03 2NOBILUS ENT Tomasz Koz(')luk
01 3Digoxin
02 1Methyl digoxin
01 1Germany
02 1India
03 2Poland
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
Registration Number : 221MF10179
Registrant's Address : 201,Empire Plaza,Mehrauli-Gurgaon Road Sultanpur,New Delhi-110 030,INDIA
Initial Date of Registration : 2009-08-07
Latest Date of Registration : 2013-03-05
Registration Number : 218MF10484
Registrant's Address : Binger Strasse 173,55216 Ingelheim am Rhein Germany
Initial Date of Registration : 2006-05-15
Latest Date of Registration : 2015-12-15
Registration Number : 228MF10002
Registrant's Address : ul. Swarzewska 45,01-821 Warszawa, POLAND
Initial Date of Registration : 2016-01-08
Latest Date of Registration : 2016-01-08
Registration Number : 226MF10104
Registrant's Address : ul. Swarzewska 45,01-821 Warszawa, POLAND
Initial Date of Registration : 2014-05-19
Latest Date of Registration : 2014-05-19
A Digoxin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Digoxin, including repackagers and relabelers. The FDA regulates Digoxin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Digoxin 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 Digoxin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Digoxin supplier is an individual or a company that provides Digoxin active pharmaceutical ingredient (API) or Digoxin finished formulations upon request. The Digoxin suppliers may include Digoxin API manufacturers, exporters, distributors and traders.
click here to find a list of Digoxin 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 Digoxin Drug Master File in Japan (Digoxin JDMF) empowers Digoxin 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 Digoxin JDMF during the approval evaluation for pharmaceutical products. At the time of Digoxin 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 Digoxin suppliers with JDMF on PharmaCompass.
We have 3 companies offering Digoxin
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