01 1Chongqing Tiandi Pharmaceutical Co., Ltd
01 1FarmChem Service Co., Ltd.
01 1Aztreonaam
01 1Blank
Registrant Name : FarmChem Service Co., Ltd.
Registration Date : 2025-02-25
Registration Number : 20250225-210-J-1786
Manufacturer Name : Chongqing Tiandi Pharmaceuti...
Manufacturer Address : No.1 Shenyang Road, Zhongzhou Avenue, Zhongxian county, Chongqing, China
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PharmaCompass offers a list of Aztreonam API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Aztreonam manufacturer or Aztreonam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aztreonam manufacturer or Aztreonam supplier.
A Aztreonam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aztreonam, including repackagers and relabelers. The FDA regulates Aztreonam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aztreonam 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 Aztreonam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Aztreonam supplier is an individual or a company that provides Aztreonam active pharmaceutical ingredient (API) or Aztreonam finished formulations upon request. The Aztreonam suppliers may include Aztreonam API manufacturers, exporters, distributors and traders.
click here to find a list of Aztreonam suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Aztreonam Drug Master File in Korea (Aztreonam KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Aztreonam. The MFDS reviews the Aztreonam KDMF as part of the drug registration process and uses the information provided in the Aztreonam KDMF to evaluate the safety and efficacy of the drug.
After submitting a Aztreonam KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Aztreonam API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Aztreonam suppliers with KDMF on PharmaCompass.
