Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1Supriya Lifescience Ltd
02 2Supriya Lifescience Ltd.
01 1Daeshin Pharmaceutical Co., Ltd.
02 1IMCD Korea Co., Ltd.
03 1Samoh Pharmaceutical Co., Ltd.
01 3Dexchlorpheniramine maleate
01 3India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : IMCD Korea Co., Ltd.
Registration Date : 2024-09-11
Registration Number : 20210302-211-J-852(2)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed. Dist-Ratnagiri, Maharashtra, Pi...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Samoh Pharmaceutical Co., Ltd.
Registration Date : 2021-03-02
Registration Number : 20210302-211-J-852
Manufacturer Name : Supriya Lifescience Ltd
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed. Dist-Ratnagiri, Maharashtra, Pi...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Daeshin Pharmaceutical Co., Ltd.
Registration Date : 2021-12-06
Registration Number : 20210302-211-J-852(1)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed. Dist-Ratnagiri, Maharashtra, Pi...
A Dexchloropheniramine Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexchloropheniramine Maleate, including repackagers and relabelers. The FDA regulates Dexchloropheniramine Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexchloropheniramine Maleate 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 Dexchloropheniramine Maleate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dexchloropheniramine Maleate supplier is an individual or a company that provides Dexchloropheniramine Maleate active pharmaceutical ingredient (API) or Dexchloropheniramine Maleate finished formulations upon request. The Dexchloropheniramine Maleate suppliers may include Dexchloropheniramine Maleate API manufacturers, exporters, distributors and traders.
click here to find a list of Dexchloropheniramine Maleate 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 Dexchloropheniramine Maleate Drug Master File in Korea (Dexchloropheniramine Maleate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Dexchloropheniramine Maleate. The MFDS reviews the Dexchloropheniramine Maleate KDMF as part of the drug registration process and uses the information provided in the Dexchloropheniramine Maleate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Dexchloropheniramine Maleate 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 Dexchloropheniramine Maleate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Dexchloropheniramine Maleate suppliers with KDMF on PharmaCompass.
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