01 1CSPC Innovation Pharmaceutical Co., Ltd.
02 1Shanghai Ethypharm Pharmaceuticals Co., Ltd.@CSPC Innovation Pharmaceutical Co., Ltd.
01 2Alvogen Korea Co., Ltd.
01 2Theophylline
01 2China
Registrant Name : Alvogen Korea Co., Ltd.
Registration Date : 2025-02-14
Registration Number : 20250214-209-J-1767
Manufacturer Name : CSPC Innovation Pharmaceutic...
Manufacturer Address : No.62 Zhangju Road, Luancheng County, Shijiazhuang City, Hebei Province, China
Registrant Name : Alvogen Korea Co., Ltd.
Registration Date : 2025-02-14
Registration Number : 20250214-209-J-1768
Manufacturer Name : Shanghai Ethypharm Pharmaceu...
Manufacturer Address : No.278, Qianyun Road, South of No.16 Bridge, State Road 318, Xujing, Qingpu District,...
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PharmaCompass offers a list of Theophylline 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 Theophylline manufacturer or Theophylline supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Theophylline manufacturer or Theophylline supplier.
PharmaCompass also assists you with knowing the Theophylline API Price utilized in the formulation of products. Theophylline API Price is not always fixed or binding as the Theophylline Price is obtained through a variety of data sources. The Theophylline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_202375 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202375, including repackagers and relabelers. The FDA regulates Tox21_202375 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202375 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 Tox21_202375 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tox21_202375 supplier is an individual or a company that provides Tox21_202375 active pharmaceutical ingredient (API) or Tox21_202375 finished formulations upon request. The Tox21_202375 suppliers may include Tox21_202375 API manufacturers, exporters, distributors and traders.
click here to find a list of Tox21_202375 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Tox21_202375 Drug Master File in Korea (Tox21_202375 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Tox21_202375. The MFDS reviews the Tox21_202375 KDMF as part of the drug registration process and uses the information provided in the Tox21_202375 KDMF to evaluate the safety and efficacy of the drug.
After submitting a Tox21_202375 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 Tox21_202375 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Tox21_202375 suppliers with KDMF on PharmaCompass.
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