Inke S.A: APIs manufacturing plant.
01 1Inke S.A.
02 1Wavelength Enterprises Ltd
03 1Chungking Carelife Pharmaceutical Co., Ltd.
04 1Hamari PFST Co., Ltd.
05 1Hamari Pharmaceuticals Co., Ltd.
06 2Hana Pharmaceutical Co. , Ltd.
07 1Hubei Haosun Pharmaceutical Co. , Ltd.
08 1Natco Pharma Limited.
09 2Qilu Pharmaceutical Co. , Ltd.
01 5Granisetron Hydrochloride
02 6Granisetron hydrochloride
01 4China
02 1France
03 1India
04 2Japan
05 2South Korea
06 1Spain
Registration Number : 218MF10350
Registrant's Address : Area Industrial del Llobregat, C/Argent 1,08755 Castellbisbal Barcelona SPAIN
Initial Date of Registration : 2006-03-17
Latest Date of Registration : 2006-12-01
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Registration Number : 218MF10399
Registrant's Address : 29 Lehi St. , Bnei-Brak 5120050, P. O. Box 2231 Israel
Initial Date of Registration : 2006-04-14
Latest Date of Registration : 2006-11-15
Registration Number : 305MF10138
Registrant's Address : Osaka Prefecture, Osaka City, Suminoe Ward, Nanko Kita 1-19-40
Initial Date of Registration : 2023-12-19
Latest Date of Registration : 2023-12-19
Registration Number : 224MF10083
Registrant's Address : 3 Hua Nanyi Road Chongqing (Changshou) Chemical Industrial Park Chongqing 401254
Initial Date of Registration : 2012-04-13
Latest Date of Registration : 2019-04-22
Registration Number : 222MF10144
Registrant's Address : 1-4-29 Shibashima, Higashiyodogawa-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2010-04-20
Latest Date of Registration : 2010-04-20
Registration Number : 305MF10130
Registrant's Address : 10F, EK Tower, 407, Teheran-ro, Gangnam-gu, Seoul, Korea
Initial Date of Registration : 2023-12-06
Latest Date of Registration : 2023-12-06
Registration Number : 301MF10013
Registrant's Address : 10F, EK Tower, 407, Teheran-ro, Gangnam-gu, Seoul, Korea
Initial Date of Registration : 2019-05-31
Latest Date of Registration : 2019-05-31
Registration Number : 225MF10063
Registrant's Address : No. 20 Juxian Road, Gedian Economic & Technology Development Area, Hubei, 436070 P. R...
Initial Date of Registration : 2013-03-27
Latest Date of Registration : 2013-03-27
Registration Number : 228MF10162
Registrant's Address : No. 317 Xinluo Road of High-tech Zone, Jinan, P. R. China
Initial Date of Registration : 2016-08-19
Latest Date of Registration : 2018-06-07
Registration Number : 302MF10064
Registrant's Address : No. 317, Xinluo Street of High Technical Zone, Jinan, P. R. China.
Initial Date of Registration : 2020-06-04
Latest Date of Registration : 2020-06-04
A Granisetron Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Granisetron Hydrochloride, including repackagers and relabelers. The FDA regulates Granisetron Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Granisetron Hydrochloride 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 Granisetron Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Granisetron Hydrochloride supplier is an individual or a company that provides Granisetron Hydrochloride active pharmaceutical ingredient (API) or Granisetron Hydrochloride finished formulations upon request. The Granisetron Hydrochloride suppliers may include Granisetron Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Granisetron Hydrochloride 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 Granisetron Hydrochloride Drug Master File in Japan (Granisetron Hydrochloride JDMF) empowers Granisetron Hydrochloride 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 Granisetron Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Granisetron Hydrochloride 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 Granisetron Hydrochloride suppliers with JDMF on PharmaCompass.
We have 9 companies offering Granisetron Hydrochloride
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