01 1Nanjing Baijingyu Pharmaceutical Co. , Ltd.
02 1Northeast Pharmaceutical Group Co. , Ltd.
03 4Yoshindo Co., Ltd.
04 1Zhejiang Apeloa Jiayuan Pharmaceutical Co. , Ltd.
01 2Chloramphenicol
02 1Chloramphenicol (N)
03 1Chloramphenicol (N) fines
04 1Chloramphenicol (production only)
05 1Day stations chloramphenicol (production only)
06 1Day stations chloramphenicol (production only) fines
01 3China
02 4Japan
Registration Number : 223MF10145
Registrant's Address : 8/F, Golden Eagle Han Zhong Garden, No. 1 Hanzhongmen street, Nanjing, China
Initial Date of Registration : 2011-09-30
Latest Date of Registration : 2011-09-30
Registration Number : 303MF10055
Registrant's Address : No. 8, Kunminghu Street, Economic & Technology Development District, Shenyang, China
Initial Date of Registration : 2021-03-30
Latest Date of Registration : 2021-03-30
Chloramphenicol (N) fine powder
Registration Number : 225MF10142
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2013-07-23
Latest Date of Registration : 2022-06-28
Registration Number : 225MF10141
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2013-07-23
Latest Date of Registration : 2022-06-28
Japanese Pharmacopoeia Chloramphenicol (for manufacturing only) fine powder
Registration Number : 218MF10435
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2009-02-10
JP Chloramphenicol (for manufacturing only)
Registration Number : 218MF10328
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-03-09
Latest Date of Registration : 2009-02-10
Chloramphenicol (for manufacturing only)
Registration Number : 219MF10197
Registrant's Address : Hengdian Industry Zone, Dongyang, Zhejiang 322118, China
Initial Date of Registration : 2007-06-08
Latest Date of Registration : 2009-02-02
A Anacetin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anacetin, including repackagers and relabelers. The FDA regulates Anacetin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anacetin 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 Anacetin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Anacetin supplier is an individual or a company that provides Anacetin active pharmaceutical ingredient (API) or Anacetin finished formulations upon request. The Anacetin suppliers may include Anacetin API manufacturers, exporters, distributors and traders.
click here to find a list of Anacetin 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 Anacetin Drug Master File in Japan (Anacetin JDMF) empowers Anacetin 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 Anacetin JDMF during the approval evaluation for pharmaceutical products. At the time of Anacetin 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 Anacetin suppliers with JDMF on PharmaCompass.
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