01 1Quimica Syntetica S. A.
02 2Zhejiang Langhua Pharmaceutical Co. , Ltd.
01 1CIPROFLOXACIN HYDROCHLORIDE
02 1Ciprofloxacin Hydrochloride
03 1Ciprofloxacin hydrochloride
01 2China
02 1Spain
Registration Number : 217MF11306
Registrant's Address : Calle Dulcinea, s/n 28805 Alcala De Henares Madrid Spain
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2022-02-10
Registration Number : 219MF10313
Registrant's Address : Zhejiang provincial chemical and medical materials base Linhai zone, Linhai, Zhejiang...
Initial Date of Registration : 2007-10-05
Latest Date of Registration : 2007-10-05
Registration Number : 223MF10021
Registrant's Address : Zhejiang provincial chemical and medical materials base Linhai zone, Linhai, Zhejiang...
Initial Date of Registration : 2011-02-08
Latest Date of Registration : 2014-05-21
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PharmaCompass offers a list of Ciprofloxacin Hydrochloride 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 Hydrochloride manufacturer or Ciprofloxacin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ciprofloxacin Hydrochloride manufacturer or Ciprofloxacin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Ciprofloxacin Hydrochloride API Price utilized in the formulation of products. Ciprofloxacin Hydrochloride API Price is not always fixed or binding as the Ciprofloxacin Hydrochloride Price is obtained through a variety of data sources. The Ciprofloxacin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cipro manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cipro, including repackagers and relabelers. The FDA regulates Cipro manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cipro 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 Cipro manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cipro supplier is an individual or a company that provides Cipro active pharmaceutical ingredient (API) or Cipro finished formulations upon request. The Cipro suppliers may include Cipro API manufacturers, exporters, distributors and traders.
click here to find a list of Cipro 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 Cipro Drug Master File in Japan (Cipro JDMF) empowers Cipro 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 Cipro JDMF during the approval evaluation for pharmaceutical products. At the time of Cipro 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 Cipro suppliers with JDMF on PharmaCompass.
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