Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1Aarti Pharmalabs limited(Unit-IV)
02 1Zhejiang Huahai Pharmaceutical Co., Ltd. Ltd
01 1Aging Life Science Co., Ltd.
02 1Menarini Korea Co., Ltd.
01 2Ranolazine
01 1China
02 1India
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Registrant Name : Aging Life Science Co., Ltd.
Registration Date : 2024-10-07
Registration Number : 434-66-ND
Manufacturer Name : Aarti Pharmalabs limited(Uni...
Manufacturer Address : Plot No: E–50, 50/1 & 59/1, MIDC, Tarapur, Taluka & District: Palghar, 401 506, Mah...
Registrant Name : Menarini Korea Co., Ltd.
Registration Date : 2020-03-13
Registration Number : 11-2-ND
Manufacturer Name : Zhejiang Huahai Pharmaceutic...
Manufacturer Address : Chuannan, Duqiao, Linhai, Zhejiang, 317016, China
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PharmaCompass offers a list of Ranolazine 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 Ranolazine manufacturer or Ranolazine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ranolazine manufacturer or Ranolazine supplier.
PharmaCompass also assists you with knowing the Ranolazine API Price utilized in the formulation of products. Ranolazine API Price is not always fixed or binding as the Ranolazine Price is obtained through a variety of data sources. The Ranolazine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Latixa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Latixa, including repackagers and relabelers. The FDA regulates Latixa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Latixa 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 Latixa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Latixa supplier is an individual or a company that provides Latixa active pharmaceutical ingredient (API) or Latixa finished formulations upon request. The Latixa suppliers may include Latixa API manufacturers, exporters, distributors and traders.
click here to find a list of Latixa 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 Latixa Drug Master File in Korea (Latixa KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Latixa. The MFDS reviews the Latixa KDMF as part of the drug registration process and uses the information provided in the Latixa KDMF to evaluate the safety and efficacy of the drug.
After submitting a Latixa 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 Latixa API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Latixa suppliers with KDMF on PharmaCompass.
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