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PharmaCompass offers a list of Urapidil 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 Urapidil Hydrochloride manufacturer or Urapidil Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Urapidil Hydrochloride manufacturer or Urapidil Hydrochloride supplier.
PharmaCompass also assists you with knowing the Urapidil Hydrochloride API Price utilized in the formulation of products. Urapidil Hydrochloride API Price is not always fixed or binding as the Urapidil Hydrochloride Price is obtained through a variety of data sources. The Urapidil Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Urapidil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urapidil, including repackagers and relabelers. The FDA regulates Urapidil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urapidil 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 Urapidil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Urapidil supplier is an individual or a company that provides Urapidil active pharmaceutical ingredient (API) or Urapidil finished formulations upon request. The Urapidil suppliers may include Urapidil API manufacturers, exporters, distributors and traders.
click here to find a list of Urapidil 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 Urapidil Drug Master File in Korea (Urapidil KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Urapidil. The MFDS reviews the Urapidil KDMF as part of the drug registration process and uses the information provided in the Urapidil KDMF to evaluate the safety and efficacy of the drug.
After submitting a Urapidil 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 Urapidil API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Urapidil suppliers with KDMF on PharmaCompass.
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