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 (+)-Chlorpheniramine maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+)-Chlorpheniramine maleate, including repackagers and relabelers. The FDA regulates (+)-Chlorpheniramine maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+)-Chlorpheniramine 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 (+)-Chlorpheniramine maleate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (+)-Chlorpheniramine maleate supplier is an individual or a company that provides (+)-Chlorpheniramine maleate active pharmaceutical ingredient (API) or (+)-Chlorpheniramine maleate finished formulations upon request. The (+)-Chlorpheniramine maleate suppliers may include (+)-Chlorpheniramine maleate API manufacturers, exporters, distributors and traders.
click here to find a list of (+)-Chlorpheniramine 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 (+)-Chlorpheniramine maleate Drug Master File in Korea ((+)-Chlorpheniramine maleate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of (+)-Chlorpheniramine maleate. The MFDS reviews the (+)-Chlorpheniramine maleate KDMF as part of the drug registration process and uses the information provided in the (+)-Chlorpheniramine maleate KDMF to evaluate the safety and efficacy of the drug.
After submitting a (+)-Chlorpheniramine 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 (+)-Chlorpheniramine maleate API can apply through the Korea Drug Master File (KDMF).
click here to find a list of (+)-Chlorpheniramine maleate suppliers with KDMF on PharmaCompass.
We have 1 companies offering (+)-Chlorpheniramine maleate
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