01 1Cambrex Profarmaco Milano S. r. l.
02 1MYUNG IN PHARM. C.O. , LTD.
03 1Sanbo Chemical Industry Co., Ltd.
01 2Triazolam
02 1Triazolam (production only)
01 1Japan
02 1South Korea
03 1U.S.A
Registration Number : 217MF11186
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2017-09-15
Triazolam (for manufacturing purposes only)
Registration Number : 220MF10242
Registrant's Address : 7-30-7 Toshima, Kita-ku, Tokyo
Initial Date of Registration : 2008-12-04
Latest Date of Registration : 2009-04-14
Registration Number : 303MF10030
Registrant's Address : 267, Hyoryeong-ro, Seocho-gu, Seoul, 06653, Republic of Korea
Initial Date of Registration : 2021-02-10
Latest Date of Registration : 2021-02-10
A Triazolam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triazolam, including repackagers and relabelers. The FDA regulates Triazolam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triazolam 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 Triazolam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triazolam supplier is an individual or a company that provides Triazolam active pharmaceutical ingredient (API) or Triazolam finished formulations upon request. The Triazolam suppliers may include Triazolam API manufacturers, exporters, distributors and traders.
click here to find a list of Triazolam 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 Triazolam Drug Master File in Japan (Triazolam JDMF) empowers Triazolam 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 Triazolam JDMF during the approval evaluation for pharmaceutical products. At the time of Triazolam 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 Triazolam suppliers with JDMF on PharmaCompass.
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