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PharmaCompass offers a list of Dexbrompheniramine Maleate 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 Dexbrompheniramine Maleate manufacturer or Dexbrompheniramine Maleate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dexbrompheniramine Maleate manufacturer or Dexbrompheniramine Maleate supplier.
PharmaCompass also assists you with knowing the Dexbrompheniramine Maleate API Price utilized in the formulation of products. Dexbrompheniramine Maleate API Price is not always fixed or binding as the Dexbrompheniramine Maleate Price is obtained through a variety of data sources. The Dexbrompheniramine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BROMPHERIL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BROMPHERIL, including repackagers and relabelers. The FDA regulates BROMPHERIL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BROMPHERIL 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 BROMPHERIL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A BROMPHERIL supplier is an individual or a company that provides BROMPHERIL active pharmaceutical ingredient (API) or BROMPHERIL finished formulations upon request. The BROMPHERIL suppliers may include BROMPHERIL API manufacturers, exporters, distributors and traders.
click here to find a list of BROMPHERIL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing BROMPHERIL as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for BROMPHERIL API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture BROMPHERIL as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain BROMPHERIL and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a BROMPHERIL NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of BROMPHERIL suppliers with NDC on PharmaCompass.
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