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PharmaCompass offers a list of Paroxetine Hydrochloride 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 Hydrochloride manufacturer or Paroxetine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Paroxetine Hydrochloride manufacturer or Paroxetine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Paroxetine Hydrochloride API Price utilized in the formulation of products. Paroxetine Hydrochloride API Price is not always fixed or binding as the Paroxetine Hydrochloride Price is obtained through a variety of data sources. The Paroxetine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Paroxetine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paroxetine, including repackagers and relabelers. The FDA regulates Paroxetine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paroxetine 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 Paroxetine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Paroxetine supplier is an individual or a company that provides Paroxetine active pharmaceutical ingredient (API) or Paroxetine finished formulations upon request. The Paroxetine suppliers may include Paroxetine API manufacturers, exporters, distributors and traders.
click here to find a list of Paroxetine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Paroxetine Drug Master File in Korea (Paroxetine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Paroxetine. The MFDS reviews the Paroxetine KDMF as part of the drug registration process and uses the information provided in the Paroxetine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Paroxetine KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Paroxetine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Paroxetine suppliers with KDMF on PharmaCompass.
We have 7 companies offering Paroxetine
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