Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1Supriya Lifescience Ltd
02 6Supriya Lifescience Ltd.
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Jimax Pharmachem Co., Ltd.
Registration Date : 2024-11-18
Registration Number : 20201217-210-J-552(6)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC, Tal.-Khed, Dist.-Ratnagiri, pin: 415 722...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Sanil Pharma Co., Ltd.
Registration Date : 2023-06-30
Registration Number : 20201217-210-J-552(4)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed, Dist- Ratnagiri 415722, Maharas...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : 아이엠씨디코리아주식회사
Registration Date : 2021-04-12
Registration Number : 20201217-210-J-552(1)
Manufacturer Name : Supriya Lifescience Ltd
Manufacturer Address : A-5/2, Lote-Parshuram Industrial Area, MIDC, Taluka-Khed, Dist.-Ratnagiri, 415722, Ma...
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 : 2020-12-17
Registration Number : 20201217-210-J-552
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed, Dist- Ratnagiri 415722, Maharas...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : (주)나르샤팜
Registration Date : 2024-09-05
Registration Number : 20201217-210-J-552(5)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed, Dist- Ratnagiri 415722, Maharas...
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 : 2021-12-08
Registration Number : 20201217-210-J-552(2)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram IndustrialArea, MIDC, Tal-Khed, Dist-Ratnagiri, 415722 Maharash...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2022-04-27
Registration Number : 20201217-210-J-552(3)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC, Tal-Khed, Dist-Ratnagiri, 415722, Mahara...
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PharmaCompass offers a list of Chlorpheniramine Maleate 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 Chlorpheniramine Maleate manufacturer or Chlorpheniramine Maleate supplier for your needs.
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PharmaCompass also assists you with knowing the Chlorpheniramine Maleate API Price utilized in the formulation of products. Chlorpheniramine Maleate API Price is not always fixed or binding as the Chlorpheniramine Maleate Price is obtained through a variety of data sources. The Chlorpheniramine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sine off manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sine off, including repackagers and relabelers. The FDA regulates Sine off manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sine off 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 Sine off supplier is an individual or a company that provides Sine off active pharmaceutical ingredient (API) or Sine off finished formulations upon request. The Sine off suppliers may include Sine off API manufacturers, exporters, distributors and traders.
click here to find a list of Sine off 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 Sine off Drug Master File in Korea (Sine off KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sine off. The MFDS reviews the Sine off KDMF as part of the drug registration process and uses the information provided in the Sine off KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sine off 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 Sine off API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Sine off suppliers with KDMF on PharmaCompass.
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