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 Levoleucovorin 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 Levoleucovorin manufacturer or Levoleucovorin supplier for your needs.
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PharmaCompass also assists you with knowing the Levoleucovorin API Price utilized in the formulation of products. Levoleucovorin API Price is not always fixed or binding as the Levoleucovorin Price is obtained through a variety of data sources. The Levoleucovorin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A L-Folinic acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-Folinic acid, including repackagers and relabelers. The FDA regulates L-Folinic acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-Folinic acid API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A L-Folinic acid supplier is an individual or a company that provides L-Folinic acid active pharmaceutical ingredient (API) or L-Folinic acid finished formulations upon request. The L-Folinic acid suppliers may include L-Folinic acid API manufacturers, exporters, distributors and traders.
click here to find a list of L-Folinic acid 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 L-Folinic acid Drug Master File in Korea (L-Folinic acid KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of L-Folinic acid. The MFDS reviews the L-Folinic acid KDMF as part of the drug registration process and uses the information provided in the L-Folinic acid KDMF to evaluate the safety and efficacy of the drug.
After submitting a L-Folinic acid 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 L-Folinic acid API can apply through the Korea Drug Master File (KDMF).
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