Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
01 2Joint Stock Company OLAIN FARM
02 1Alembic Pharmaceuticals Limited
03 1Cheer Fine Pharmaceutical Co. , Ltd.
04 1DNP Fine Chemicals Utsunomiya Co., Ltd.
05 1LUPIN LIMITED.
06 1Procos S. p. A.
07 3UBE Inc.
08 1Zhejiang Apeloa Kangyu Pharmaceutical Co. , Ltd.
Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
Registration Number : 230MF10048
Registrant's Address : 5 Rupnicu Street, Olain, LV-2114, Latvia
Initial Date of Registration : 2018-03-30
Latest Date of Registration : 2018-03-30
Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
Registration Number : 230MF10010
Registrant's Address : 5 Rupnicu Street, Olain, LV-2114, Latvia
Initial Date of Registration : 2018-01-24
Latest Date of Registration : 2018-01-24
A Namenda manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Namenda, including repackagers and relabelers. The FDA regulates Namenda manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Namenda 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 Namenda manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Namenda supplier is an individual or a company that provides Namenda active pharmaceutical ingredient (API) or Namenda finished formulations upon request. The Namenda suppliers may include Namenda API manufacturers, exporters, distributors and traders.
click here to find a list of Namenda 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 Namenda Drug Master File in Japan (Namenda JDMF) empowers Namenda 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 Namenda JDMF during the approval evaluation for pharmaceutical products. At the time of Namenda 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 Namenda suppliers with JDMF on PharmaCompass.
We have 8 companies offering Namenda
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
