Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
01 2M/s. Synnat Pharma Private Limited
02 1M/s CIpla Limited
03 2M/s Hetero Drugs Limited
04 1M/s JPN Pharma Pvt. Ltd
05 1M/s Sun Pharmaceutical Industries Ltd
06 1M/s Synthimed Labs Private Limited
07 1M/s. Apitoria Pharma Private Limited
08 1M/sMacleods pharmaceuticals Limited
Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
Risedronate Sodium 2,5-hydrate BP/Ph. Eur.
Date of Issue : 2024-05-22
Valid Till : 2027-02-07
Written Confirmation Number : WC-0301
Address of the Firm : Plot No. 60A, Jawaharlal Nehru Pharma City, Parawada Mandal, Anakapalli District...
Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
Date of Issue : 2024-05-22
Valid Till : 2027-02-07
Written Confirmation Number : WC-0301
Address of the Firm : Plot No. 60A, Jawaharlal Nehru Pharma City, Parawada Mandal, Anakapalli District...
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A Risedronate Sodium API manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Risedronate Sodium API, including repackagers and relabelers. The FDA regulates Risedronate Sodium API manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Risedronate Sodium API 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 Risedronate Sodium API supplier is an individual or a company that provides Risedronate Sodium API active pharmaceutical ingredient (API) or Risedronate Sodium API finished formulations upon request. The Risedronate Sodium API suppliers may include Risedronate Sodium API API manufacturers, exporters, distributors and traders.
click here to find a list of Risedronate Sodium API suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Risedronate Sodium API written confirmation (Risedronate Sodium API WC) is an official document issued by a regulatory agency to a Risedronate Sodium API manufacturer, verifying that the manufacturing facility of a Risedronate Sodium API active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Risedronate Sodium API APIs or Risedronate Sodium API finished pharmaceutical products to another nation, regulatory agencies frequently require a Risedronate Sodium API WC (written confirmation) as part of the regulatory process.
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