01 1M/s. Dishman Pharmaceuticals and Chemicals Ltd.
02 1M/s. Parabolic Drugs Ltd.,
01 1Strontium Renelate IH
02 1Strontium Renelate Octahydrate
01 1WC-0135
02 1WC-267
01 2India
Date of Issue : 2019-07-22
Valid Till : 2022-07-02
Written Confirmation Number : WC-0135
Address of the Firm : Survey No. 47, Paiki Sub Plot No. 1, Village Lodariyal, Taluka Sanand, Dist. Ahm...
Strontium Renelate Octahydrate
Date of Issue : 2014-02-28
Valid Till : 2017-02-17
Written Confirmation Number : WC-267
Address of the Firm : Village- Chachrauli, Tehsil- Derabassi, Dist-S.A.S Nagar(Mohali)
A Distrontium Renelate Octahydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Distrontium Renelate Octahydrate, including repackagers and relabelers. The FDA regulates Distrontium Renelate Octahydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Distrontium Renelate Octahydrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Distrontium Renelate Octahydrate supplier is an individual or a company that provides Distrontium Renelate Octahydrate active pharmaceutical ingredient (API) or Distrontium Renelate Octahydrate finished formulations upon request. The Distrontium Renelate Octahydrate suppliers may include Distrontium Renelate Octahydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Distrontium Renelate Octahydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Distrontium Renelate Octahydrate written confirmation (Distrontium Renelate Octahydrate WC) is an official document issued by a regulatory agency to a Distrontium Renelate Octahydrate manufacturer, verifying that the manufacturing facility of a Distrontium Renelate Octahydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Distrontium Renelate Octahydrate APIs or Distrontium Renelate Octahydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Distrontium Renelate Octahydrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Distrontium Renelate Octahydrate suppliers with Written Confirmation (WC) on PharmaCompass.
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