01 1Mac-Chem Products (India) Pvt.Ltd.
01 1(주)에스지바이오켐
01 1Hydrocortisone sodium succinate
01 1India
Hydrocortisone sodium succinate
Registrant Name : (주)에스지바이오켐
Registration Date : 2025-03-07
Registration Number : 20250307-210-J-1693
Manufacturer Name : Mac-Chem Products (India) Pv...
Manufacturer Address : N-211/2/10, MIDC, Boisar, Dist. Palghar 401 506, State Maharashtra, India
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PharmaCompass offers a list of Hydrocortisone Sodium Succinate 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 Hydrocortisone Sodium Succinate manufacturer or Hydrocortisone Sodium Succinate supplier for your needs.
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PharmaCompass also assists you with knowing the Hydrocortisone Sodium Succinate API Price utilized in the formulation of products. Hydrocortisone Sodium Succinate API Price is not always fixed or binding as the Hydrocortisone Sodium Succinate Price is obtained through a variety of data sources. The Hydrocortisone Sodium Succinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nositrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nositrol, including repackagers and relabelers. The FDA regulates Nositrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nositrol 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 Nositrol supplier is an individual or a company that provides Nositrol active pharmaceutical ingredient (API) or Nositrol finished formulations upon request. The Nositrol suppliers may include Nositrol API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Nositrol Drug Master File in Korea (Nositrol KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Nositrol. The MFDS reviews the Nositrol KDMF as part of the drug registration process and uses the information provided in the Nositrol KDMF to evaluate the safety and efficacy of the drug.
After submitting a Nositrol 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 Nositrol API can apply through the Korea Drug Master File (KDMF).
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