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01 1Divi’s Laboratories
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01 1Carbidopa (IP/BP/USP/Ph. Eur)
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01 1WC-0030
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01 1India
Date of Issue : 2019-06-17
Valid Till : 2022-06-16
Written Confirmation Number : WC-0030
Address of the Firm : Unit-II, Annavaram(Post), Chippada Village, Beemunipatnam Mandal, Visakhapatan...
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PharmaCompass offers a list of Carbidopa 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 Carbidopa manufacturer or Carbidopa supplier for your needs.
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PharmaCompass also assists you with knowing the Carbidopa API Price utilized in the formulation of products. Carbidopa API Price is not always fixed or binding as the Carbidopa Price is obtained through a variety of data sources. The Carbidopa Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RYTARY manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RYTARY, including repackagers and relabelers. The FDA regulates RYTARY manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RYTARY 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 RYTARY manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RYTARY supplier is an individual or a company that provides RYTARY active pharmaceutical ingredient (API) or RYTARY finished formulations upon request. The RYTARY suppliers may include RYTARY API manufacturers, exporters, distributors and traders.
click here to find a list of RYTARY suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A RYTARY written confirmation (RYTARY WC) is an official document issued by a regulatory agency to a RYTARY manufacturer, verifying that the manufacturing facility of a RYTARY active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting RYTARY APIs or RYTARY finished pharmaceutical products to another nation, regulatory agencies frequently require a RYTARY WC (written confirmation) as part of the regulatory process.
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