Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
01 1Interquim S. A.
02 1Aurobindo Pharma Limited
03 1Cambrex Karlskoga AB
04 1ERREGIERRE S. p. A.
05 1Shodhana Laboratories Limited
06 1Viyash Life Sciences Private Limited
01 5Rivastigmine
02 1Rivastigmine (manufacturing only)
01 3India
02 1Italy
03 1Spain
04 1U.S.A
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
Registration Number : 301MF10032
Registrant's Address : Joan Buscala, 10 E-08173 Sant Cugat del Valles, Barcelona, Spain
Initial Date of Registration : 2019-07-19
Latest Date of Registration : 2019-07-19
Registration Number : 301MF10019
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad Telangana, India
Initial Date of Registration : 2019-06-18
Latest Date of Registration : 2020-05-12
Registration Number : 303MF10138
Registrant's Address : SE-691 85 Karlskoga, SWEDEN
Initial Date of Registration : 2021-08-25
Latest Date of Registration : 2024-12-04
Registration Number : 228MF10192
Registrant's Address : VIA F. BARACCA 19-24060 SAN PAOLO D'ARGON (BERGAMO) ITALY
Initial Date of Registration : 2016-10-05
Latest Date of Registration : 2016-10-05
Rivastigmine (for manufacturing purposes only)
Registration Number : 301MF10057
Registrant's Address : 6B, 6th Floor, Krishe' Block, Krishe' Sapphire, Madhapur, Hyderabad - 500 081, Telang...
Initial Date of Registration : 2019-08-29
Latest Date of Registration : 2019-08-29
Registration Number : 230MF10164
Registrant's Address : Plot No. 290, Srivalli's Corporate, Road No. 6, Kakatiya Hills, Madhapur, Hyderabad-5...
Initial Date of Registration : 2018-12-04
Latest Date of Registration : 2020-05-15
A Rivastigmine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rivastigmine, including repackagers and relabelers. The FDA regulates Rivastigmine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rivastigmine 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 Rivastigmine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rivastigmine supplier is an individual or a company that provides Rivastigmine active pharmaceutical ingredient (API) or Rivastigmine finished formulations upon request. The Rivastigmine suppliers may include Rivastigmine API manufacturers, exporters, distributors and traders.
click here to find a list of Rivastigmine 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 Rivastigmine Drug Master File in Japan (Rivastigmine JDMF) empowers Rivastigmine 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 Rivastigmine JDMF during the approval evaluation for pharmaceutical products. At the time of Rivastigmine 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 Rivastigmine suppliers with JDMF on PharmaCompass.
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