SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
01 1SCI Pharmtech, Inc.
02 3Anlon healthcare private limited
03 1Cheer Fine Pharmaceutical Co. , Ltd.
04 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
05 2Daiichi Sankyo Chemical Pharma Co., Ltd.
06 1Daiwa Pharmaceutical Industries Co., Ltd.
07 1Dijia Pharmaceutical Group Co. , Ltd.
08 1Fujian Huitian Biological Pharmaceutical Co. ,Ltd
09 3HUBEI XUNDA PHARMACEUTICAL CO. , LTD.
10 1HUBEI XUNDA PHARMACEUTICAL CO. ,LTD
11 1Hamari PFST Co., Ltd.
12 1Hanseo Chemical Co. , Ltd.
13 8KOLON LIFE SCIENCE, INC.
14 1KUKJEON PHARMACEUTICAL Co. , Ltd.
15 1Ohara Pharmaceutical Co., Ltd.
16 1Pen Tsao Chemical Industry Ltd.
17 1SAM-OH PHARM. C.O. , LTD.
18 1Saurav Chemicals Limited
19 1Seven Star Pharmaceutical Co. , Ltd.
20 1Shin Poong Pharm. Co. , Ltd.
21 1Tateyama Chemical Co., Ltd.
22 2Yamamoto Chemical Industry Co., Ltd.
23 2Yoshindo Co., Ltd.
24 1Yungjin Pharm. Co. ,Ltd
25 1Zhejiang Apeloa Jiayuan Pharmaceutical Co. , Ltd.
26 1Zhejiang Apeloa Jiayuan Pharmaceutical Co. ,Ltd
27 3Zhejiang Starry Pharmaceutical Co. ,Ltd
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Registration Number : 223MF10166
Registrant's Address : No. 61, Ln. 309, Haihu N. Rd. , Luzhu Dist. , Taoyuan City 33856, Taiwan
Initial Date of Registration : 2011-11-28
Latest Date of Registration : 2011-11-28
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PharmaCompass offers a list of Loxoprofen Sodium 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 Loxoprofen Sodium manufacturer or Loxoprofen Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Loxoprofen Sodium API Price utilized in the formulation of products. Loxoprofen Sodium API Price is not always fixed or binding as the Loxoprofen Sodium Price is obtained through a variety of data sources. The Loxoprofen Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Loxoprofen Sodium Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Loxoprofen Sodium Dihydrate, including repackagers and relabelers. The FDA regulates Loxoprofen Sodium Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Loxoprofen Sodium Dihydrate 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 Loxoprofen Sodium Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Loxoprofen Sodium Dihydrate supplier is an individual or a company that provides Loxoprofen Sodium Dihydrate active pharmaceutical ingredient (API) or Loxoprofen Sodium Dihydrate finished formulations upon request. The Loxoprofen Sodium Dihydrate suppliers may include Loxoprofen Sodium Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Loxoprofen Sodium Dihydrate 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 Loxoprofen Sodium Dihydrate Drug Master File in Japan (Loxoprofen Sodium Dihydrate JDMF) empowers Loxoprofen Sodium Dihydrate 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 Loxoprofen Sodium Dihydrate JDMF during the approval evaluation for pharmaceutical products. At the time of Loxoprofen Sodium Dihydrate 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 Loxoprofen Sodium Dihydrate suppliers with JDMF on PharmaCompass.
We have 25 companies offering Loxoprofen Sodium Dihydrate
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