01 1Dansk Salt A/S
02 1Dansk salt A/S
03 1Salinen Austria AG
01 1Hans Korea Co., Ltd.
02 1Meditip Co., Ltd.
03 1Parmarine Co., Ltd.
01 1Sodium Chloride
02 2Sodium chloride
01 1Austria
02 2U.S.A
Registrant Name : Hans Korea Co., Ltd.
Registration Date : 2023-04-07
Registration Number : 20210527-211-J-824(1)
Manufacturer Name : Dansk Salt A/S
Manufacturer Address : Hadsundvej 17, DK-9550 Mariager, Denmark
Registrant Name : Meditip Co., Ltd.
Registration Date : 2021-05-27
Registration Number : 20210527-211-J-824
Manufacturer Name : Dansk salt A/S
Manufacturer Address : Hadsundvej 17, Mariager 9550, Denmark
Registrant Name : Parmarine Co., Ltd.
Registration Date : 2025-03-11
Registration Number : 20250311-211-J-1775
Manufacturer Name : Salinen Austria AG
Manufacturer Address : Steinkogelstraße 30 4802 Ebensee
25
PharmaCompass offers a list of Sodium Chloride 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 Sodium Chloride manufacturer or Sodium Chloride supplier for your needs.
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A DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3 supplier is an individual or a company that provides DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3 active pharmaceutical ingredient (API) or DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3 finished formulations upon request. The DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3 suppliers may include DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3 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 DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3 Drug Master File in Korea (DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3. The MFDS reviews the DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3 KDMF as part of the drug registration process and uses the information provided in the DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3 KDMF to evaluate the safety and efficacy of the drug.
After submitting a DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3 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 DIALYTE LM/ DEXTROSE 1.5% IN PLASTIC CONTAINER-3 API can apply through the Korea Drug Master File (KDMF).
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