01 1Shandong Anhong Pharmaceutical Co., Ltd.
01 1Sampung Pharmachem Co., Ltd.
01 1Etoposide
01 1China
Registrant Name : Sampung Pharmachem Co., Ltd.
Registration Date : 2025-05-23
Registration Number : 20250523-209-J-1883
Manufacturer Name : Shandong Anhong Pharmaceutic...
Manufacturer Address : No. 29 Huayuan Street Linyi County, Dezhou, Shandong, China
86
PharmaCompass offers a list of Etoposide 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 Etoposide manufacturer or Etoposide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Etoposide manufacturer or Etoposide supplier.
A Etoposide Teva manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etoposide Teva, including repackagers and relabelers. The FDA regulates Etoposide Teva manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etoposide Teva 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 Etoposide Teva manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Etoposide Teva supplier is an individual or a company that provides Etoposide Teva active pharmaceutical ingredient (API) or Etoposide Teva finished formulations upon request. The Etoposide Teva suppliers may include Etoposide Teva API manufacturers, exporters, distributors and traders.
click here to find a list of Etoposide Teva 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 Etoposide Teva Drug Master File in Korea (Etoposide Teva KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Etoposide Teva. The MFDS reviews the Etoposide Teva KDMF as part of the drug registration process and uses the information provided in the Etoposide Teva KDMF to evaluate the safety and efficacy of the drug.
After submitting a Etoposide Teva 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 Etoposide Teva API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Etoposide Teva suppliers with KDMF on PharmaCompass.
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