Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
01 1Metrochem API Pvt. Ltd.
02 1RUYUAN HEC PHARM CO. , LTD.
01 2Teneligliptin Hydrobromide Hydrate
01 1China
02 1India
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
Teneligliptin Hydrobromide Hydrate
Registration Number : 307MF10084
Registrant's Address : Flat No. 302, Bhanu Enclave, Sunder Nagar, Erragadda, Hyderabad - 500038, Telangana, ...
Initial Date of Registration : 2025-07-16
Latest Date of Registration : 2025-07-16
Teneligliptin hydrobromide hydrate
Registration Number : 307MF10106
Registrant's Address : Xiaba Development Zone, Ruyuan County, Shaoguan City, Guangdong Province, P. R. China
Initial Date of Registration : 2025-08-21
Latest Date of Registration : 2025-08-21
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A tenelia manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of tenelia, including repackagers and relabelers. The FDA regulates tenelia manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. tenelia 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 tenelia manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A tenelia supplier is an individual or a company that provides tenelia active pharmaceutical ingredient (API) or tenelia finished formulations upon request. The tenelia suppliers may include tenelia API manufacturers, exporters, distributors and traders.
click here to find a list of tenelia suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 tenelia Drug Master File in Japan (tenelia JDMF) empowers tenelia 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 tenelia JDMF during the approval evaluation for pharmaceutical products. At the time of tenelia 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 tenelia suppliers with JDMF on PharmaCompass.
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