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 : 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 : 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 : 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
59
PharmaCompass offers a list of Aciclovir API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Aciclovir manufacturer or Aciclovir supplier for your needs.
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PharmaCompass also assists you with knowing the Aciclovir API Price utilized in the formulation of products. Aciclovir API Price is not always fixed or binding as the Aciclovir Price is obtained through a variety of data sources. The Aciclovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sitavig manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sitavig, including repackagers and relabelers. The FDA regulates Sitavig manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sitavig 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 Sitavig manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sitavig supplier is an individual or a company that provides Sitavig active pharmaceutical ingredient (API) or Sitavig finished formulations upon request. The Sitavig suppliers may include Sitavig API manufacturers, exporters, distributors and traders.
click here to find a list of Sitavig 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 Sitavig Drug Master File in Japan (Sitavig JDMF) empowers Sitavig 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 Sitavig JDMF during the approval evaluation for pharmaceutical products. At the time of Sitavig 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 Sitavig suppliers with JDMF on PharmaCompass.
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