Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1Aarti Pharmalabs Limited
02 2Siegfried St. Vulbas SAS
01 1AstraZeneca Korea Ltd.
02 1Chong Kun Dang Co., Ltd.
03 1Yuhan Corporation
01 3Bamboo terol hydrochloride
01 1India
02 2Switzerland
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Registrant Name : Chong Kun Dang Co., Ltd.
Registration Date : 2005-09-15
Registration Number : 20050915-38-B-209-04
Manufacturer Name : Aarti Pharmalabs Limited
Manufacturer Address : Plot No. D-53, Phase-II MIDC, Kalyan-Shill Road, Dombivali(East), District Thane - 42...
Registrant Name : Yuhan Corporation
Registration Date : 2012-03-23
Registration Number : 20050831-38-B-100-01(1)
Manufacturer Name : Siegfried St. Vulbas SAS
Manufacturer Address : Parc Industriel de la Plaine de I`Ain 530 Allee de la Luye 01150 SAINT-VULBAS, France
Registrant Name : AstraZeneca Korea Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-38-B-100-01
Manufacturer Name : Siegfried St. Vulbas SAS
Manufacturer Address : Parc Industriel de la Plaine de I`Ain 530 Allee de la Luye 01150 SAINT-VULBAS, France
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PharmaCompass offers a list of Bambuterol Hydrochloride 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 Bambuterol Hydrochloride manufacturer or Bambuterol Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Bambuterol Hydrochloride API Price utilized in the formulation of products. Bambuterol Hydrochloride API Price is not always fixed or binding as the Bambuterol Hydrochloride Price is obtained through a variety of data sources. The Bambuterol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxeol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxeol, including repackagers and relabelers. The FDA regulates Oxeol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxeol 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 Oxeol supplier is an individual or a company that provides Oxeol active pharmaceutical ingredient (API) or Oxeol finished formulations upon request. The Oxeol suppliers may include Oxeol API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Oxeol Drug Master File in Korea (Oxeol KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Oxeol. The MFDS reviews the Oxeol KDMF as part of the drug registration process and uses the information provided in the Oxeol KDMF to evaluate the safety and efficacy of the drug.
After submitting a Oxeol 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 Oxeol API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Oxeol suppliers with KDMF on PharmaCompass.
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