Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
01 1Malladi Drugs & Pharmaceuticals Ltd
02 1Siegfried PharmaChemikalien Minden GmbH
01 1CTC Bio Co., Ltd.
02 1Kukjeon Pharmaceutical Co., Ltd.
01 2Pseudoephedrine sulfate
01 1India
02 1Switzerland
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2008-02-28
Registration Number : 20080228-75-B-253-03
Manufacturer Name : Malladi Drugs & Pharmaceutic...
Manufacturer Address : 7B&7C, SIPCOT Industrial Complex, Ranipet-632 403, Ranipet District, Tamil Nadu, Indi...
Registrant Name : CTC Bio Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-75-B-198-01
Manufacturer Name : Siegfried PharmaChemikalien ...
Manufacturer Address : Karlstrasße 15-39, 42-44 32423 Minden, Germany
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PharmaCompass offers a list of Pseudoephedrine Sulfate 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 Pseudoephedrine Sulfate manufacturer or Pseudoephedrine Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Pseudoephedrine Sulfate API Price utilized in the formulation of products. Pseudoephedrine Sulfate API Price is not always fixed or binding as the Pseudoephedrine Sulfate Price is obtained through a variety of data sources. The Pseudoephedrine Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pseudoephedrine Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pseudoephedrine Sulfate, including repackagers and relabelers. The FDA regulates Pseudoephedrine Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pseudoephedrine Sulfate 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 Pseudoephedrine Sulfate supplier is an individual or a company that provides Pseudoephedrine Sulfate active pharmaceutical ingredient (API) or Pseudoephedrine Sulfate finished formulations upon request. The Pseudoephedrine Sulfate suppliers may include Pseudoephedrine Sulfate API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Pseudoephedrine Sulfate Drug Master File in Korea (Pseudoephedrine Sulfate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Pseudoephedrine Sulfate. The MFDS reviews the Pseudoephedrine Sulfate KDMF as part of the drug registration process and uses the information provided in the Pseudoephedrine Sulfate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Pseudoephedrine Sulfate 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 Pseudoephedrine Sulfate API can apply through the Korea Drug Master File (KDMF).
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