01 2IFF N&H Norway AS
01 1Parmarine Co., Ltd.
02 1YuYu Pharmaceutical Co., Ltd.
01 2Sodium alginate
01 2U.S.A
Registrant Name : Parmarine Co., Ltd.
Registration Date : 2022-03-28
Registration Number : 20220328-211-J-1256
Manufacturer Name : IFF N&H Norway AS
Manufacturer Address : Steinhaugvegen 1, VORMEDAL, NO-5545, Norway
Registrant Name : YuYu Pharmaceutical Co., Ltd.
Registration Date : 2022-09-28
Registration Number : 20220328-211-J-1256(1)
Manufacturer Name : IFF N&H Norway AS
Manufacturer Address : Steinhauvegen 1, VORMEDAL, NO-5545, Norway
A Sodium Alginate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Alginate, including repackagers and relabelers. The FDA regulates Sodium Alginate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Alginate 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 Sodium Alginate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Alginate supplier is an individual or a company that provides Sodium Alginate active pharmaceutical ingredient (API) or Sodium Alginate finished formulations upon request. The Sodium Alginate suppliers may include Sodium Alginate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Alginate 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 Sodium Alginate Drug Master File in Korea (Sodium Alginate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sodium Alginate. The MFDS reviews the Sodium Alginate KDMF as part of the drug registration process and uses the information provided in the Sodium Alginate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sodium Alginate 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 Sodium Alginate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sodium Alginate suppliers with KDMF on PharmaCompass.
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