01 1Zambon Group SpA
01 1Samoh Pharmaceutical Co., Ltd.
01 1Oxaprozin
01 1Italy
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-54-C-180-03
Manufacturer Name : Zambon Group SpA
Manufacturer Address : Via Dovaro 36045 Almisano di Lonigo (Vicenza) (Via della Chimica, 9, 36100 Vicenza), ...
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PharmaCompass offers a list of Oxaprozin 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 Oxaprozin manufacturer or Oxaprozin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Oxaprozin manufacturer or Oxaprozin supplier.
PharmaCompass also assists you with knowing the Oxaprozin API Price utilized in the formulation of products. Oxaprozin API Price is not always fixed or binding as the Oxaprozin Price is obtained through a variety of data sources. The Oxaprozin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Wy-21,743 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Wy-21,743, including repackagers and relabelers. The FDA regulates Wy-21,743 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Wy-21,743 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Wy-21,743 supplier is an individual or a company that provides Wy-21,743 active pharmaceutical ingredient (API) or Wy-21,743 finished formulations upon request. The Wy-21,743 suppliers may include Wy-21,743 API manufacturers, exporters, distributors and traders.
click here to find a list of Wy-21,743 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 Wy-21,743 Drug Master File in Korea (Wy-21,743 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Wy-21,743. The MFDS reviews the Wy-21,743 KDMF as part of the drug registration process and uses the information provided in the Wy-21,743 KDMF to evaluate the safety and efficacy of the drug.
After submitting a Wy-21,743 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 Wy-21,743 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Wy-21,743 suppliers with KDMF on PharmaCompass.
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