01 1M/s Harman Finochem Limited
02 1M/s Harman Finochem limited
03 1M/s Swati Spentose Private Limited
01 1Phenytoin BP/EP/USP
02 1Phenytoin EP
03 1Phenytoin EP/USP
01 1WC-0044
02 1WC-0045nA2
03 1WC-0165
01 3India
Date of Issue : 2022-06-06
Valid Till : 2025-07-21
Written Confirmation Number : WC-0044
Address of the Firm : Plot No. A-100, A-100/1, A-100/2 & D-1, M.I.D.C Ind. Area, Shendra, Aurangabad-4...
Date of Issue : 2022-08-06
Valid Till : 2025-07-21
Written Confirmation Number : WC-0045nA2
Address of the Firm : Plot No. E-7, E-8, E-9, MIDC Industrial Area, Chikalthana, Aurangabad-431006
Date of Issue : 2022-06-15
Valid Till : 2025-07-07
Written Confirmation Number : WC-0165
Address of the Firm : Plot No. A-1/2102 & 2103, Phase-III, G.I.D.C Vapi-396195, Valsad, Gujarat, India
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PharmaCompass offers a list of Phenytoin 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 Phenytoin manufacturer or Phenytoin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Phenytoin manufacturer or Phenytoin supplier.
PharmaCompass also assists you with knowing the Phenytoin API Price utilized in the formulation of products. Phenytoin API Price is not always fixed or binding as the Phenytoin Price is obtained through a variety of data sources. The Phenytoin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neosidantoina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neosidantoina, including repackagers and relabelers. The FDA regulates Neosidantoina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neosidantoina 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 Neosidantoina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Neosidantoina supplier is an individual or a company that provides Neosidantoina active pharmaceutical ingredient (API) or Neosidantoina finished formulations upon request. The Neosidantoina suppliers may include Neosidantoina API manufacturers, exporters, distributors and traders.
click here to find a list of Neosidantoina suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Neosidantoina written confirmation (Neosidantoina WC) is an official document issued by a regulatory agency to a Neosidantoina manufacturer, verifying that the manufacturing facility of a Neosidantoina active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Neosidantoina APIs or Neosidantoina finished pharmaceutical products to another nation, regulatory agencies frequently require a Neosidantoina WC (written confirmation) as part of the regulatory process.
click here to find a list of Neosidantoina suppliers with Written Confirmation (WC) on PharmaCompass.
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