IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
01 1M/s. IOL Chemicals and Pharmaceuticals Ltd.
02 1M/s Solara Active Pharma Sciences Limited
03 1Solara Active Pharma Sciences Limited
01 1Ibuprofen Lysinate IH
02 1Ibuprofen Lysine
03 1Ibuprofen Lysine IH
01 1WC-0004
02 1WC-0126-Amended
03 1WC-0127
01 3India
IOL Chemicals is an innovation-driven bulk drug, Intermediate and Specialty Chemicals company.
Date of Issue : 2025-02-27
Valid Till : 2027-03-17
Written Confirmation Number : WC-0004
Address of the Firm : Village Fatehgarh Channa Mansa Road, (Trident Complex), Barnala, District Barnal...
Date of Issue : 2022-09-30
Valid Till : 2025-08-04
Written Confirmation Number : WC-0127
Address of the Firm : A1/B, SIPCOT Industrial Complex, Kudikadu, Cuddalore-607 005
Date of Issue : 2022-07-15
Valid Till : 2025-07-25
Written Confirmation Number : WC-0126-Amended
Address of the Firm : R.S No.33 and 34 Mathur Road Periyakalapet, Punducherry India
39
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A 57469-76-8 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 57469-76-8, including repackagers and relabelers. The FDA regulates 57469-76-8 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 57469-76-8 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 57469-76-8 supplier is an individual or a company that provides 57469-76-8 active pharmaceutical ingredient (API) or 57469-76-8 finished formulations upon request. The 57469-76-8 suppliers may include 57469-76-8 API manufacturers, exporters, distributors and traders.
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A 57469-76-8 written confirmation (57469-76-8 WC) is an official document issued by a regulatory agency to a 57469-76-8 manufacturer, verifying that the manufacturing facility of a 57469-76-8 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 57469-76-8 APIs or 57469-76-8 finished pharmaceutical products to another nation, regulatory agencies frequently require a 57469-76-8 WC (written confirmation) as part of the regulatory process.
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