01 1CENTAUR PHARMACEUTICALS PRIVATE LTD.
02 1Cambrex Profarmaco Milano S. r. l.
03 1Ohara Pharmaceutical Co., Ltd.
04 1UBE Co., Ltd.
01 3Etizolam
02 1Japanese Pharmacopoeia etizolam (production only)
01 1India
02 2Japan
03 1U.S.A
Registration Number : 222MF10191
Registrant's Address : 1978-96 Ogushi, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2010-07-07
Latest Date of Registration : 2010-07-07
Registration Number : 218MF11013
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2024-07-11
Registration Number : 225MF10155
Registrant's Address : “CENTAUR HOUSE”, NEAR GRAND HYATT, SHANTI NAGAR, VAKOLA, SANTACRUZ (EAST), MUMBAI...
Initial Date of Registration : 2013-08-12
Latest Date of Registration : 2013-08-12
Japanese Pharmacopoeia Etizolam (for manufacturing purposes only)
Registration Number : 217MF11220
Registrant's Address : 121-15 Torii-no, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2007-12-19
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PharmaCompass offers a list of Etizolam 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 Etizolam manufacturer or Etizolam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etizolam manufacturer or Etizolam supplier.
PharmaCompass also assists you with knowing the Etizolam API Price utilized in the formulation of products. Etizolam API Price is not always fixed or binding as the Etizolam Price is obtained through a variety of data sources. The Etizolam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AHR 3219 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AHR 3219, including repackagers and relabelers. The FDA regulates AHR 3219 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AHR 3219 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 AHR 3219 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AHR 3219 supplier is an individual or a company that provides AHR 3219 active pharmaceutical ingredient (API) or AHR 3219 finished formulations upon request. The AHR 3219 suppliers may include AHR 3219 API manufacturers, exporters, distributors and traders.
click here to find a list of AHR 3219 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 AHR 3219 Drug Master File in Japan (AHR 3219 JDMF) empowers AHR 3219 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 AHR 3219 JDMF during the approval evaluation for pharmaceutical products. At the time of AHR 3219 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 AHR 3219 suppliers with JDMF on PharmaCompass.
We have 4 companies offering AHR 3219
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