01 2Excella GmbH & Co. KG
02 1Wanbury Limited
03 1Zhejiang Huahai Pharmaceutical Co., Ltd.
01 1PAROXETINE MESYLATE
02 3Paroxetine Mesylate
01 1China
02 1India
03 2Luxembourg
NDC Package Code : 46014-1125
Start Marketing Date : 2017-10-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46014-1097
Start Marketing Date : 2017-01-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62350-0074
Start Marketing Date : 2016-02-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64220-174
Start Marketing Date : 2013-11-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Paroxetine Mesylate 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 Paroxetine Mesylate manufacturer or Paroxetine Mesylate supplier for your needs.
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PharmaCompass also assists you with knowing the Paroxetine Mesylate API Price utilized in the formulation of products. Paroxetine Mesylate API Price is not always fixed or binding as the Paroxetine Mesylate Price is obtained through a variety of data sources. The Paroxetine Mesylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BRISDELLE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BRISDELLE, including repackagers and relabelers. The FDA regulates BRISDELLE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BRISDELLE 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 BRISDELLE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A BRISDELLE supplier is an individual or a company that provides BRISDELLE active pharmaceutical ingredient (API) or BRISDELLE finished formulations upon request. The BRISDELLE suppliers may include BRISDELLE API manufacturers, exporters, distributors and traders.
click here to find a list of BRISDELLE 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 BRISDELLE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for BRISDELLE 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 BRISDELLE 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 BRISDELLE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a BRISDELLE NDC to their finished compounded human drug products, they may choose to do so.
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