01 1Aurobindo Pharma Limited
02 1Dipharma Francis S. r. l.
03 2Kyongbo Pharmaceutical Co. , Ltd.
04 2Tateyama Chemical Co., Ltd.
01 3Entacapone
02 2Entacapone
03 1Entacapone "Tateyama"
01 1India
02 1Italy
03 2Japan
04 2South Korea
Registration Number : 227MF10029
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad Andhra Pradesh, India
Initial Date of Registration : 2015-01-23
Latest Date of Registration : 2015-11-20
Registration Number : 227MF10070
Registrant's Address : Via Bissone, 5, 20021-Baranzate, Milano, Italy
Initial Date of Registration : 2015-03-12
Latest Date of Registration : 2015-03-12
Registration Number : 302MF10042
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2020-04-02
Latest Date of Registration : 2020-04-02
Registration Number : 227MF10041
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2015-02-09
Latest Date of Registration : 2015-02-09
Registration Number : 226MF10119
Registrant's Address : 1133 Ōe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2014-06-18
Latest Date of Registration : 2015-11-20
Registration Number : 230MF10071
Registrant's Address : 1133 Ōe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2018-06-07
Latest Date of Registration : 2018-06-07
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PharmaCompass offers a list of Entacapone API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Entacapone manufacturer or Entacapone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Entacapone manufacturer or Entacapone supplier.
A C14H15N3O5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C14H15N3O5, including repackagers and relabelers. The FDA regulates C14H15N3O5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C14H15N3O5 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 C14H15N3O5 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A C14H15N3O5 supplier is an individual or a company that provides C14H15N3O5 active pharmaceutical ingredient (API) or C14H15N3O5 finished formulations upon request. The C14H15N3O5 suppliers may include C14H15N3O5 API manufacturers, exporters, distributors and traders.
click here to find a list of C14H15N3O5 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 C14H15N3O5 Drug Master File in Japan (C14H15N3O5 JDMF) empowers C14H15N3O5 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 C14H15N3O5 JDMF during the approval evaluation for pharmaceutical products. At the time of C14H15N3O5 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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We have 4 companies offering C14H15N3O5
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