Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1AARTI INDUSTRIES LIMITED.
01 1Salmeterol Xinafoate
01 1India
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Registration Number : 227MF10240
Registrant's Address : 71, UDYOG KSHETRA, ULND-GOREGAON LINK ROAD, MULUND (W), MUMBAI 400080, INDIA
Initial Date of Registration : 2015-09-29
Latest Date of Registration : 2015-09-29
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PharmaCompass offers a list of Salmeterol Xinafoate 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 Salmeterol Xinafoate manufacturer or Salmeterol Xinafoate supplier for your needs.
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PharmaCompass also assists you with knowing the Salmeterol Xinafoate API Price utilized in the formulation of products. Salmeterol Xinafoate API Price is not always fixed or binding as the Salmeterol Xinafoate Price is obtained through a variety of data sources. The Salmeterol Xinafoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Salmeterol Xinafoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Salmeterol Xinafoate, including repackagers and relabelers. The FDA regulates Salmeterol Xinafoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Salmeterol Xinafoate 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 Salmeterol Xinafoate supplier is an individual or a company that provides Salmeterol Xinafoate active pharmaceutical ingredient (API) or Salmeterol Xinafoate finished formulations upon request. The Salmeterol Xinafoate suppliers may include Salmeterol Xinafoate API manufacturers, exporters, distributors and traders.
click here to find a list of Salmeterol Xinafoate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Salmeterol Xinafoate Drug Master File in Japan (Salmeterol Xinafoate JDMF) empowers Salmeterol Xinafoate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Salmeterol Xinafoate JDMF during the approval evaluation for pharmaceutical products. At the time of Salmeterol Xinafoate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Salmeterol Xinafoate suppliers with JDMF on PharmaCompass.
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