01 2Olon S. p. A.
02 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A.
03 1Tianish Laboratories Private Limited
04 1Yung Zip Chemical Ind. Co. , Ltd.
05 2Zhejiang Charioteer Pharmaceutical Co. , Ltd.
06 1Zhejiang Zhebei Pharmaceutical Co. , Ltd.
01 2Aciclovir
02 6Acyclovir
01 3China
02 3Italy
03 1Taiwan
04 1U.S.A
Registration Number : 218MF10098
Registrant's Address : Tongyuanxi, Dazhan, Xianju, Zhejiang Province, 317321, P. R. China.
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2014-10-27
Registration Number : 306MF10109
Registrant's Address : Tongyuanxi, Dazhan, Xianju, Zhejiang Province, 317321, P. R. China.
Initial Date of Registration : 2024-08-07
Latest Date of Registration : 2024-08-07
Registration Number : 218MF10016
Registrant's Address : Strada Rivoltana, km 6/7, 20053 Rodano (MI), Italy
Initial Date of Registration : 2006-01-27
Latest Date of Registration : 2022-01-11
Registration Number : 303MF10178
Registrant's Address : Strada Rivoltana, km 6/7, 20053 Rodano (MI), Italy
Initial Date of Registration : 2021-12-15
Latest Date of Registration : 2021-12-15
Registration Number : 217MF10746
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2015-07-13
Registration Number : 218MF10974
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2006-12-01
Latest Date of Registration : 2013-01-18
Registration Number : 221MF10178
Registrant's Address : 59, You Shih Road, Youth Industrial District, Dajia, Taichung, Taiwan 43767, R. O. C.
Initial Date of Registration : 2009-08-07
Latest Date of Registration : 2017-07-25
Registration Number : 221MF10074
Registrant's Address : 66 Guoshan Road, Xinshi Town, Deqing, Zhejiang, China
Initial Date of Registration : 2009-04-14
Latest Date of Registration : 2009-04-14
17
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A DivK1c_000185 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DivK1c_000185, including repackagers and relabelers. The FDA regulates DivK1c_000185 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DivK1c_000185 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A DivK1c_000185 supplier is an individual or a company that provides DivK1c_000185 active pharmaceutical ingredient (API) or DivK1c_000185 finished formulations upon request. The DivK1c_000185 suppliers may include DivK1c_000185 API manufacturers, exporters, distributors and traders.
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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 DivK1c_000185 Drug Master File in Japan (DivK1c_000185 JDMF) empowers DivK1c_000185 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 DivK1c_000185 JDMF during the approval evaluation for pharmaceutical products. At the time of DivK1c_000185 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 6 companies offering DivK1c_000185
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