Neuland Laboratories- A dedicated 100% API provider.
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01 1Neuland Laboratories Limited.
02 1FUJIFILM Toyama Chemical Co., Ltd.
03 2Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
04 1Pharmacostech CO. ,LTD
05 1Shiono Finesse Co., Ltd.
06 1Uquifa Mexico, S. A. de C. V.
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01 2Ciprofloxacin
02 2Japanese Pharmacopoeia toss ciprofloxacin tosylate salt hydrate production-only
03 1Supra Tasuto tosylate
04 1Toss ciprofloxacin tosylate salt hydrate
05 1Toss ciprofloxacin tosylate salt hydrate (pulverized product)
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01 1India
02 4Japan
03 1South Korea
04 1Spain
Registration Number : 219MF10357
Registrant's Address : 11th Floor (5th Office Level), Phoenix IVY Building, Plot No. 573A-Ⅲ, Road No. 82, ...
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2016-05-13
Registration Number : 220MF10086
Registrant's Address : 2-14-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2008-03-18
Latest Date of Registration : 2012-10-29
Japanese Pharmacopoeia Tosufloxacin Tosilate Hydrate For manufacturing only
Registration Number : 221MF10286
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2009-12-22
Latest Date of Registration : 2009-12-22
Japanese Pharmacopoeia Tosufloxacin Tosilate Hydrate For manufacturing only
Registration Number : 229MF10174
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2017-09-04
Latest Date of Registration : 2017-09-04
Tosufloxacin tosilate hydrate (ground product)
Registration Number : 228MF10147
Registrant's Address : 47, Jeyakdanji-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Republic of Korea
Initial Date of Registration : 2016-08-03
Latest Date of Registration : 2016-08-03
Registration Number : 227MF10118
Registrant's Address : Osaka Prefecture, Osaka City, Chuo Ward, Doshomachi 3-1-6
Initial Date of Registration : 2015-04-21
Latest Date of Registration : 2020-11-26
Registration Number : 219MF10080
Registrant's Address : Calle 37 Este No. 126, CIVAC, 62578, Jiutepec, Morelos, Mexico
Initial Date of Registration : 2007-03-14
Latest Date of Registration : 2007-03-14
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PharmaCompass offers a list of Ciprofloxacin 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 Ciprofloxacin manufacturer or Ciprofloxacin supplier for your needs.
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PharmaCompass also assists you with knowing the Ciprofloxacin API Price utilized in the formulation of products. Ciprofloxacin API Price is not always fixed or binding as the Ciprofloxacin Price is obtained through a variety of data sources. The Ciprofloxacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A A-8526 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of A-8526, including repackagers and relabelers. The FDA regulates A-8526 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. A-8526 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 A-8526 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A A-8526 supplier is an individual or a company that provides A-8526 active pharmaceutical ingredient (API) or A-8526 finished formulations upon request. The A-8526 suppliers may include A-8526 API manufacturers, exporters, distributors and traders.
click here to find a list of A-8526 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 A-8526 Drug Master File in Japan (A-8526 JDMF) empowers A-8526 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 A-8526 JDMF during the approval evaluation for pharmaceutical products. At the time of A-8526 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 A-8526 suppliers with JDMF on PharmaCompass.
We have 6 companies offering A-8526
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