01 1Bayer AG
01 1Bayer Korea Ltd.
01 1IOB-DTPA
01 1Germany
Registrant Name : Bayer Korea Ltd.
Registration Date : 2006-05-11
Registration Number : 309-3-ND
Manufacturer Name : Bayer AG
Manufacturer Address : Ernst-Schering-Straße 14 59192 Bergkamen, Germany
90
PharmaCompass offers a list of Pentetic Acid 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 Pentetic Acid manufacturer or Pentetic Acid supplier for your needs.
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PharmaCompass also assists you with knowing the Pentetic Acid API Price utilized in the formulation of products. Pentetic Acid API Price is not always fixed or binding as the Pentetic Acid Price is obtained through a variety of data sources. The Pentetic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DTPA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DTPA, including repackagers and relabelers. The FDA regulates DTPA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DTPA 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 DTPA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DTPA supplier is an individual or a company that provides DTPA active pharmaceutical ingredient (API) or DTPA finished formulations upon request. The DTPA suppliers may include DTPA API manufacturers, exporters, distributors and traders.
click here to find a list of DTPA 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 DTPA Drug Master File in Korea (DTPA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DTPA. The MFDS reviews the DTPA KDMF as part of the drug registration process and uses the information provided in the DTPA KDMF to evaluate the safety and efficacy of the drug.
After submitting a DTPA 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 DTPA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of DTPA suppliers with KDMF on PharmaCompass.
