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