01 1Amicogen (China) Biopharm Co. , Ltd.
02 1Hamari PFST Co., Ltd.
03 1INIST ST CO. , LTD.
04 1JEIL PHARMACEUTICAL CO. , LTD.
05 3KOLON LIFE SCIENCE, INC.
06 1Nippon Kayaku Co., Ltd.
07 1Pharmaxyn Laboratories Ltd.
08 1Ranbaxy Laboratories Limited
09 2Shanghai Tianwei Biopharmaceutical Co., Ltd.
10 1Tokuyama Corporation
11 1YUHAN CORPORATION
12 2Zhejiang HISOAR Pharmaceutical Co. ,Ltd
01 1Day stations
02 1Japanese Pharmacopoeia voglibose
03 8Voglibose
04 1Voglibose "KOA"
05 1Voglibose "NK"
06 1Voglibose "hamari Y"
07 1Voglibose (C)
08 1Voglibose (N)
09 1Voglibose SN
01 6China
02 1India
03 3Japan
04 6South Korea
Registration Number : 229MF10143
Registrant's Address : No. 1688 Shixian Road, Jining City, Shandong Province
Initial Date of Registration : 2017-07-25
Latest Date of Registration : 2017-07-25
Japanese Pharmacopoeia Voglibose
Registration Number : 223MF10028
Registrant's Address : 500, Sinnae-ro, Geumwang-eup, Eumseong-gun, Chungcheongbuk-do, Korea
Initial Date of Registration : 2011-02-25
Latest Date of Registration : 2019-05-08
Registration Number : 226MF10227
Registrant's Address : 343, Sapyeong-daero, Seocho-gu, Seoul, Korea
Initial Date of Registration : 2014-12-08
Latest Date of Registration : 2014-12-08
Registration Number : 222MF10132
Registrant's Address : 110, MAGOKDONG-RO, GANGSEO-GU, SEOUL, KOREA
Initial Date of Registration : 2010-04-12
Latest Date of Registration : 2010-04-12
Registration Number : 303MF10056
Registrant's Address : 110, MAGOKDONG-RO, GANGSEO-GU, SEOUL, KOREA
Initial Date of Registration : 2021-03-30
Latest Date of Registration : 2024-03-27
Registration Number : 227MF10165
Registrant's Address : No. 9, Minpu Road, Qingyang, Jiangyin, Wuxi, Jiangsu, 214401 China
Initial Date of Registration : 2015-06-18
Latest Date of Registration : 2015-06-18
Registration Number : 224MF10201
Registrant's Address : Plot No. 90, Sector 32, Gurgaon, Haryana 122 001, India
Initial Date of Registration : 2012-10-03
Latest Date of Registration : 2012-10-03
Registration Number : 227MF10108
Registrant's Address : No. 4258 Jindu Road, Shanghai, China
Initial Date of Registration : 2015-04-09
Latest Date of Registration : 2015-04-09
Registration Number : 217MF11015
Registrant's Address : No. 100 Waisha Branch Rd. , Jiaojiang, Taizhou, Zhejiang, China
Initial Date of Registration : 2005-11-21
Latest Date of Registration : 2011-06-15
Registration Number : 302MF10094
Registrant's Address : No. 100 Waisha Branch Rd. , Jiaojiang, Taizhou, Zhejiang, China
Initial Date of Registration : 2020-08-05
Latest Date of Registration : 2021-04-27
A Voglibose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Voglibose, including repackagers and relabelers. The FDA regulates Voglibose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Voglibose 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 Voglibose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Voglibose supplier is an individual or a company that provides Voglibose active pharmaceutical ingredient (API) or Voglibose finished formulations upon request. The Voglibose suppliers may include Voglibose API manufacturers, exporters, distributors and traders.
click here to find a list of Voglibose 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 Voglibose Drug Master File in Japan (Voglibose JDMF) empowers Voglibose 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 Voglibose JDMF during the approval evaluation for pharmaceutical products. At the time of Voglibose 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 Voglibose suppliers with JDMF on PharmaCompass.
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