01 1M/s. Centauar Pharmacerticals Pvt. Ltd.,
01 1Methyl phenidate BP/EP/USP
01 1WC-0107
01 1India
Date of Issue : 2022-06-08
Valid Till : 2025-06-25
Written Confirmation Number : WC-0107
Address of the Firm : Plot No. 75/76, Chikhloli, MIDC, Ambernath (W), Dist- Thane 421501 Maharashtra ...
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PharmaCompass offers a list of Methylphenidate 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 Methylphenidate manufacturer or Methylphenidate supplier for your needs.
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PharmaCompass also assists you with knowing the Methylphenidate API Price utilized in the formulation of products. Methylphenidate API Price is not always fixed or binding as the Methylphenidate Price is obtained through a variety of data sources. The Methylphenidate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Equasym XL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Equasym XL, including repackagers and relabelers. The FDA regulates Equasym XL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Equasym XL 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 Equasym XL supplier is an individual or a company that provides Equasym XL active pharmaceutical ingredient (API) or Equasym XL finished formulations upon request. The Equasym XL suppliers may include Equasym XL API manufacturers, exporters, distributors and traders.
click here to find a list of Equasym XL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Equasym XL written confirmation (Equasym XL WC) is an official document issued by a regulatory agency to a Equasym XL manufacturer, verifying that the manufacturing facility of a Equasym XL active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Equasym XL APIs or Equasym XL finished pharmaceutical products to another nation, regulatory agencies frequently require a Equasym XL WC (written confirmation) as part of the regulatory process.
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