Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1M/s Supriya Lifescience Ltd
02 1M/s Divs Laboratories Limited
03 1M/s Exemed Pharmaceuticals
04 1M/s Hy-Gro Chemicals Pharmtek Private Limiteds
05 1M/s Melody healthcare Pvt Ltd
06 1M/s Solara Active Pharma Sciences Limited
07 1M/s Wanbury Limited
08 1M/s.Srini Pharmaceuticals Private Limited
09 1M/sKreative Organics Private limited
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Dextromethorphan Hydrobromide BP/EP/USP
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0218n
Address of the Firm : A-5/2, Late Parshuram Industrial Area, MIDC, Tal-Khed, Dist. Ratnagiri-415 722, ...
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PharmaCompass offers a list of Dextromethorphan Hydrobromide 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 Dextromethorphan Hydrobromide manufacturer or Dextromethorphan Hydrobromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dextromethorphan Hydrobromide manufacturer or Dextromethorphan Hydrobromide supplier.
PharmaCompass also assists you with knowing the Dextromethorphan Hydrobromide API Price utilized in the formulation of products. Dextromethorphan Hydrobromide API Price is not always fixed or binding as the Dextromethorphan Hydrobromide Price is obtained through a variety of data sources. The Dextromethorphan Hydrobromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Levomethorphan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levomethorphan, including repackagers and relabelers. The FDA regulates Levomethorphan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levomethorphan 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 Levomethorphan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levomethorphan supplier is an individual or a company that provides Levomethorphan active pharmaceutical ingredient (API) or Levomethorphan finished formulations upon request. The Levomethorphan suppliers may include Levomethorphan API manufacturers, exporters, distributors and traders.
click here to find a list of Levomethorphan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Levomethorphan written confirmation (Levomethorphan WC) is an official document issued by a regulatory agency to a Levomethorphan manufacturer, verifying that the manufacturing facility of a Levomethorphan active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Levomethorphan APIs or Levomethorphan finished pharmaceutical products to another nation, regulatory agencies frequently require a Levomethorphan WC (written confirmation) as part of the regulatory process.
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