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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A Serevent Inhaler and Disks manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Serevent Inhaler and Disks, including repackagers and relabelers. The FDA regulates Serevent Inhaler and Disks manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Serevent Inhaler and Disks 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 Serevent Inhaler and Disks supplier is an individual or a company that provides Serevent Inhaler and Disks active pharmaceutical ingredient (API) or Serevent Inhaler and Disks finished formulations upon request. The Serevent Inhaler and Disks suppliers may include Serevent Inhaler and Disks API manufacturers, exporters, distributors and traders.
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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 Serevent Inhaler and Disks Drug Master File in Japan (Serevent Inhaler and Disks JDMF) empowers Serevent Inhaler and Disks 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 Serevent Inhaler and Disks JDMF during the approval evaluation for pharmaceutical products. At the time of Serevent Inhaler and Disks JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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