01 1Nandu Chemical Industries
01 1Big Farms Co., Ltd.
01 1sodium acetate hydrate
01 1India
Registrant Name : Big Farms Co., Ltd.
Registration Date : 2025-06-04
Registration Number : 20250604-211-J-1919
Manufacturer Name : Nandu Chemical Industries
Manufacturer Address : N-12, Industrial Estate, Gokul Road, HUBLI-580030, Karnataka, INDIA
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PharmaCompass offers a list of Sodium Acetate 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 Sodium Acetate manufacturer or Sodium Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Acetate API Price utilized in the formulation of products. Sodium Acetate API Price is not always fixed or binding as the Sodium Acetate Price is obtained through a variety of data sources. The Sodium Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SODIUM ACETATE, USP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SODIUM ACETATE, USP, including repackagers and relabelers. The FDA regulates SODIUM ACETATE, USP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SODIUM ACETATE, USP 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 SODIUM ACETATE, USP supplier is an individual or a company that provides SODIUM ACETATE, USP active pharmaceutical ingredient (API) or SODIUM ACETATE, USP finished formulations upon request. The SODIUM ACETATE, USP suppliers may include SODIUM ACETATE, USP 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 SODIUM ACETATE, USP Drug Master File in Korea (SODIUM ACETATE, USP KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of SODIUM ACETATE, USP. The MFDS reviews the SODIUM ACETATE, USP KDMF as part of the drug registration process and uses the information provided in the SODIUM ACETATE, USP KDMF to evaluate the safety and efficacy of the drug.
After submitting a SODIUM ACETATE, USP 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 ACETATE, USP API can apply through the Korea Drug Master File (KDMF).
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