Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
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01 1Supriya Lifescience Ltd
02 6Supriya Lifescience Ltd.
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01 1(주)나르샤팜
02 1Daeshin Pharmaceutical Co., Ltd.
03 1Jimax Pharmachem Co., Ltd.
04 1Kukjeon Pharmaceutical Co., Ltd.
05 1Samoh Pharmaceutical Co., Ltd.
06 1Sanil Pharma Co., Ltd.
07 1아이엠씨디코리아주식회사
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01 7Chlorpheniramine maleate
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01 7India
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 Chlor-trimeton 12 hour manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlor-trimeton 12 hour, including repackagers and relabelers. The FDA regulates Chlor-trimeton 12 hour manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlor-trimeton 12 hour 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 Chlor-trimeton 12 hour manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlor-trimeton 12 hour supplier is an individual or a company that provides Chlor-trimeton 12 hour active pharmaceutical ingredient (API) or Chlor-trimeton 12 hour finished formulations upon request. The Chlor-trimeton 12 hour suppliers may include Chlor-trimeton 12 hour API manufacturers, exporters, distributors and traders.
click here to find a list of Chlor-trimeton 12 hour 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 Chlor-trimeton 12 hour Drug Master File in Korea (Chlor-trimeton 12 hour KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Chlor-trimeton 12 hour. The MFDS reviews the Chlor-trimeton 12 hour KDMF as part of the drug registration process and uses the information provided in the Chlor-trimeton 12 hour KDMF to evaluate the safety and efficacy of the drug.
After submitting a Chlor-trimeton 12 hour 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 Chlor-trimeton 12 hour API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Chlor-trimeton 12 hour suppliers with KDMF on PharmaCompass.
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