01 2Apitoria Pharma Private Limited Unit-I
02 1IPCA Laboratories Limited
03 3Ipca Laboratories Limited
04 1Myungin Pharmaceutical Co., Ltd.
05 1Piramal Pharma Limited
06 1Thermo Fisher Scientific Cork Limited
07 2Tianish Laboratories Private Limited (Unit-1)
08 1Zhejiang Haisen Pharmaceutical Co., Ltd
09 1Zhejiang Huahai Pharmaceutical Co., Ltd.
10 1Zydus Lifesciences Limited
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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, 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.
A Paroxat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paroxat, including repackagers and relabelers. The FDA regulates Paroxat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paroxat 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 Paroxat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Paroxat supplier is an individual or a company that provides Paroxat active pharmaceutical ingredient (API) or Paroxat finished formulations upon request. The Paroxat suppliers may include Paroxat API manufacturers, exporters, distributors and traders.
click here to find a list of Paroxat suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Paroxat Drug Master File in Korea (Paroxat KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Paroxat. The MFDS reviews the Paroxat KDMF as part of the drug registration process and uses the information provided in the Paroxat KDMF to evaluate the safety and efficacy of the drug.
After submitting a Paroxat 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 Paroxat API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Paroxat suppliers with KDMF on PharmaCompass.
We have 9 companies offering Paroxat
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