01 1LUPIN LIMITED.
02 1Sanwa Chemical Co., Ltd.
03 1Themis Medicare Ltd.
01 2Ethambutol hydrochloride
02 1Japanese Pharmacopoeia hydrochloric acid ethambutol (production only)
01 2India
02 1Japan
Registration Number : 225MF10019
Registrant's Address : Kalpataru Inspire, 3rd Floor, Off Western Express Highway, Santacruz (East), Mumbai 4...
Initial Date of Registration : 2013-02-05
Latest Date of Registration : 2013-02-05
Japanese Pharmacopoeia Ethambutol Hydrochloride (for manufacturing only)
Registration Number : 218MF10556
Registrant's Address : 24-8 Tamura 9-chome, Hiratsuka City, Kanagawa Prefecture
Initial Date of Registration : 2006-06-02
Latest Date of Registration : 2009-03-16
Registration Number : 221MF10232
Registrant's Address : 11/12, Udyog Nagar, S. V. Road, Goregaon-West, Mumbai-400104, India
Initial Date of Registration : 2009-10-26
Latest Date of Registration : 2009-10-26
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PharmaCompass offers a list of Ethambutol Dihydrochloride 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 Ethambutol Dihydrochloride manufacturer or Ethambutol Dihydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethambutol Dihydrochloride manufacturer or Ethambutol Dihydrochloride supplier.
PharmaCompass also assists you with knowing the Ethambutol Dihydrochloride API Price utilized in the formulation of products. Ethambutol Dihydrochloride API Price is not always fixed or binding as the Ethambutol Dihydrochloride Price is obtained through a variety of data sources. The Ethambutol Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E1011 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E1011, including repackagers and relabelers. The FDA regulates E1011 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E1011 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 E1011 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E1011 supplier is an individual or a company that provides E1011 active pharmaceutical ingredient (API) or E1011 finished formulations upon request. The E1011 suppliers may include E1011 API manufacturers, exporters, distributors and traders.
click here to find a list of E1011 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 E1011 Drug Master File in Japan (E1011 JDMF) empowers E1011 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 E1011 JDMF during the approval evaluation for pharmaceutical products. At the time of E1011 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 E1011 suppliers with JDMF on PharmaCompass.
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