01 1F. I. S. Fabrica Italiana Sintetici S. p. A.
02 2Ipca Laboratories Limited
03 1SMS Lifesciences India Limited
01 1"Japan-station" furosemide (production only)
02 3Furosemide
01 3India
02 1Italy
Registration Number : 217MF10541
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2023-11-08
Registration Number : 225MF10191
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (W), Mumbai 400 067, India
Initial Date of Registration : 2013-10-09
Latest Date of Registration : 2013-10-09
Japanese Pharmacopoeia Furosemide (for manufacturing purposes only)
Registration Number : 218MF10276
Registrant's Address : 48, Kandivli Industrial Estate. Kandivli (W), Mumbai 400 067 India
Initial Date of Registration : 2006-02-23
Latest Date of Registration : 2007-01-22
Registration Number : 307MF10145
Registrant's Address : Plot No. 19-III, Road No. 71, Opp. Bharatiya Vidya Bhavan Public School, Jubilee Hill...
Initial Date of Registration : 2025-12-04
Latest Date of Registration : 2025-12-04
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PharmaCompass offers a list of Furosemide 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 Furosemide manufacturer or Furosemide supplier for your needs.
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PharmaCompass also assists you with knowing the Furosemide API Price utilized in the formulation of products. Furosemide API Price is not always fixed or binding as the Furosemide Price is obtained through a variety of data sources. The Furosemide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A C12H11ClN2O5S manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C12H11ClN2O5S, including repackagers and relabelers. The FDA regulates C12H11ClN2O5S manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C12H11ClN2O5S API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A C12H11ClN2O5S supplier is an individual or a company that provides C12H11ClN2O5S active pharmaceutical ingredient (API) or C12H11ClN2O5S finished formulations upon request. The C12H11ClN2O5S suppliers may include C12H11ClN2O5S API manufacturers, exporters, distributors and traders.
click here to find a list of C12H11ClN2O5S 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 C12H11ClN2O5S Drug Master File in Japan (C12H11ClN2O5S JDMF) empowers C12H11ClN2O5S 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 C12H11ClN2O5S JDMF during the approval evaluation for pharmaceutical products. At the time of C12H11ClN2O5S JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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