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