01 1ABC Farmaceutici SPA (Unibios Division)
02 1Asia Chemical Industries Ltd. Teva-Tech Site
03 1Hanseo Cam Co., Ltd.
04 1Hubei Yitai Pharmaceutical Co.,Ltd
05 1Mylan Laboratories Limited
06 2Mylan Laboratories Limited (Unit-7)
07 1Olon SpA
08 6Recordati Industria Chimica Farmaceutica SpA
09 1Shanghai Pharma Group Changzhou Kony Pharmaceutical Co., Ltd.
10 1Sicor Societa' Italiana Corticosteroidi SRL
11 1Union Quimico Farmaceutica SA
12 2Union Quimico Farmaceutica, SA
13 1Union quimco farmaceutica, SA
14 1XINXIANG PHARMACEUTICAL CO.,LTD
15 1Yung Zip Chemical Ind. Co., Ltd.
16 3Zhejiang Charioteer Pharmaceutical Co., Ltd.
17 12Zhejiang Charioteer Pharmaceutical Co., Ltd.@Zhejiang Charioteer Pharmaceutical Co., Ltd.
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.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Aciclovir Drug Master File in Korea (Aciclovir KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Aciclovir. The MFDS reviews the Aciclovir KDMF as part of the drug registration process and uses the information provided in the Aciclovir KDMF to evaluate the safety and efficacy of the drug.
After submitting a Aciclovir KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Aciclovir API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Aciclovir suppliers with KDMF on PharmaCompass.
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