01 1Matrix Pharmacorp Private Limited
02 2Olon S. p. A.
03 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A.
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. 14, 99 and 100, IDA, Pashamylaram Phase-II, Patancheru, Sangareddy District ...
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
PharmaCompass offers a list of Acyclovir 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 Acyclovir manufacturer or Acyclovir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Acyclovir manufacturer or Acyclovir supplier.
PharmaCompass also assists you with knowing the Acyclovir API Price utilized in the formulation of products. Acyclovir API Price is not always fixed or binding as the Acyclovir Price is obtained through a variety of data sources. The Acyclovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aciclovier manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aciclovier, including repackagers and relabelers. The FDA regulates Aciclovier manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aciclovier 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 Aciclovier manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aciclovier supplier is an individual or a company that provides Aciclovier active pharmaceutical ingredient (API) or Aciclovier finished formulations upon request. The Aciclovier suppliers may include Aciclovier API manufacturers, exporters, distributors and traders.
click here to find a list of Aciclovier 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 Aciclovier Drug Master File in Japan (Aciclovier JDMF) empowers Aciclovier 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 Aciclovier JDMF during the approval evaluation for pharmaceutical products. At the time of Aciclovier 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 Aciclovier suppliers with JDMF on PharmaCompass.
We have 6 companies offering Aciclovier
Get in contact with the supplier of your choice:
