01 1MOLCLONE LABS PRIVATE LIMITED
01 1Agerson Bio Co., Ltd.
01 1sodium levofolinate
01 1India
Registrant Name : Agerson Bio Co., Ltd.
Registration Date : 2025-04-21
Registration Number : 20250421-210-J-1540
Manufacturer Name : MOLCLONE LABS PRIVATE LIMITE...
Manufacturer Address : No. 2/22 (SURVEY NO. 173/1A, 173/2 AND 173/3), SIRUMATHUR VALLAGE, PADAPPAI, SRIPERUM...
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PharmaCompass offers a list of Sodium Levofolinate 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 Sodium Levofolinate manufacturer or Sodium Levofolinate supplier for your needs.
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A Sodium Levofolinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Levofolinate, including repackagers and relabelers. The FDA regulates Sodium Levofolinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Levofolinate 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 Sodium Levofolinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Sodium Levofolinate supplier is an individual or a company that provides Sodium Levofolinate active pharmaceutical ingredient (API) or Sodium Levofolinate finished formulations upon request. The Sodium Levofolinate suppliers may include Sodium Levofolinate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Levofolinate 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 Sodium Levofolinate Drug Master File in Korea (Sodium Levofolinate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sodium Levofolinate. The MFDS reviews the Sodium Levofolinate KDMF as part of the drug registration process and uses the information provided in the Sodium Levofolinate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sodium Levofolinate 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 Sodium Levofolinate API can apply through the Korea Drug Master File (KDMF).
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