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
A Aciclovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aciclovir, including repackagers and relabelers. The FDA regulates Aciclovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aciclovir 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 Aciclovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aciclovir supplier is an individual or a company that provides Aciclovir active pharmaceutical ingredient (API) or Aciclovir finished formulations upon request. The Aciclovir suppliers may include Aciclovir API manufacturers, exporters, distributors and traders.
click here to find a list of Aciclovir 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 Aciclovir Drug Master File in Japan (Aciclovir JDMF) empowers Aciclovir 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 Aciclovir JDMF during the approval evaluation for pharmaceutical products. At the time of Aciclovir 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 Aciclovir suppliers with JDMF on PharmaCompass.
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